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dbVar

Database of genomic structural variation

nsv5663318

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: 98 SVs from 17 studies. See in: genome view

Submitted genomic56,269,073-56,269,073

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5663318	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	56,269,073	56,269,073
nsv5663318	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	56,302,985	56,302,985

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17097865	insertion	HG01505	Sequencing	Sequence alignment	1,109

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17097865	Submitted genomic		NC_000016.10:g.562 69073_56269074ins5 5	GRCh38 (hg38)		NC_000016.10	Chr16	56,269,073	56,269,073
nssv17097865	Remapped	Perfect	NC_000016.9:g.5630 2985_56302986ins55	GRCh37.p13	First Pass	NC_000016.9	Chr16	56,302,985	56,302,985

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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