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dbVar

Database of genomic structural variation

nsv5655939

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert et al. 2021

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: 753 SVs from 80 studies. See in: genome view

Submitted genomic54,239,128-54,239,128

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5655939	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	54,239,128	54,239,128
nsv5655939	Remapped	Perfect	GRCh37.p13	PATCHES	First Pass	NW_004166865.1	Chr19\|NW_0 04166865.1	213,495	213,495

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17106090	insertion	HG03486	Sequencing	Sequence alignment	4,355

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17106090	Submitted genomic		NC_000019.10:g.542 39128_54239129ins1 9212	GRCh38 (hg38)		NC_000019.10	Chr19	54,239,128	54,239,128
nssv17106090	Remapped	Perfect	NW_004166865.1:g.2 13495_213496ins192 12	GRCh37.p13	First Pass	NW_004166865.1	Chr19\|NW_0 04166865.1	213,495	213,495

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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