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dbVar

Database of genomic structural variation

nsv5626528

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: 92 SVs from 21 studies. See in: genome view

Submitted genomic39,253,540-39,253,540

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5626528	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	39,253,540	39,253,540
nsv5626528	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	39,253,642	39,253,642

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17126543	insertion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17126543	Submitted genomic		NC_000005.10:g.392 53540_39253541ins2 97	GRCh38 (hg38)		NC_000005.10	Chr5	39,253,540	39,253,540
nssv17126543	Remapped	Perfect	NC_000005.9:g.3925 3642_39253643ins29 7	GRCh37.p13	First Pass	NC_000005.9	Chr5	39,253,642	39,253,642

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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