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dbVar

Database of genomic structural variation

nsv5671672

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: 269 SVs from 31 studies. See in: genome view

Submitted genomic14,980,613-14,980,613

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5671672	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	14,980,613	14,980,613
nsv5671672	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	16,352,934	16,352,934

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17118238	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17118238	Submitted genomic		NC_000021.9:g.1498 0613_14980614ins33 5	GRCh38 (hg38)		NC_000021.9	Chr21	14,980,613	14,980,613
nssv17118238	Remapped	Perfect	NC_000021.8:g.1635 2934_16352935ins33 5	GRCh37.p13	First Pass	NC_000021.8	Chr21	16,352,934	16,352,934

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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