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dbVar

Database of genomic structural variation

nsv4944044

Organism: Homo sapiens

Study:nstd200 (Abel et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:156,895

Publication(s):Abel et al. 2020

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 491 SVs from 57 studies. See in: genome view

Submitted genomic139,615,061-139,772,122

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4944044	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	139,615,155 (-94, +2)	139,772,049 (-2, +73)
nsv4944044	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	140,536,309 (-94, +2)	140,693,203 (-2, +73)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16473485	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16473485	Submitted genomic		NC_000004.12:g.(13 9615061_139615157) _(139772047_139772 122)dup	GRCh38 (hg38)		NC_000004.12	Chr4	139,615,155 (-94, +2)	139,772,049 (-2, +73)
nssv16473485	Remapped	Perfect	NC_000004.11:g.(14 0536215_140536311) _(140693201_140693 276)dup	GRCh37.p13	First Pass	NC_000004.11	Chr4	140,536,309 (-94, +2)	140,693,203 (-2, +73)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16473485	<0.001	1	29246

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