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dbVar

Database of genomic structural variation

nsv5639747

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: 171 SVs from 48 studies. See in: genome view

Submitted genomic29,069,515-29,069,515

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5639747	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	29,069,515	29,069,515
nsv5639747	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	29,069,622	29,069,622

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17134411	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17134411	Submitted genomic		NC_000005.10:g.290 69515_29069516ins9 128	GRCh38 (hg38)		NC_000005.10	Chr5	29,069,515	29,069,515
nssv17134411	Remapped	Perfect	NC_000005.9:g.2906 9622_29069623ins91 28	GRCh37.p13	First Pass	NC_000005.9	Chr5	29,069,622	29,069,622

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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