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dbVar

Database of genomic structural variation

nsv5577656

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:43,365

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: 895 SVs from 82 studies. See in: genome view

Submitted genomic130,044,539-130,087,903

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5577656	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	130,044,539	130,087,903
nsv5577656	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	129,763,382	129,806,746

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17129294	deletion	SAMN00006580	Sequencing	Sequence alignment	9,409

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17129294	Submitted genomic		NC_000003.12:g.130 044539_130087903de lC	GRCh38 (hg38)		NC_000003.12	Chr3	130,044,539	130,087,903
nssv17129294	Remapped	Perfect	NC_000003.11:g.129 763382_129806746de lC	GRCh37.p13	First Pass	NC_000003.11	Chr3	129,763,382	129,806,746

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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