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dbVar

Database of genomic structural variation

nsv5627374

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

Submitted genomic432,672-432,672

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5627374	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	432,672	432,672
nsv5627374	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	472,655	472,655

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17139649	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
nssv17139649	Submitted genomic		NC_000007.14:g.432 672_432673ins292	GRCh38 (hg38)		NC_000007.14	Chr7	432,672	432,672
nssv17139649	Remapped	Perfect	NC_000007.13:g.472 655_472656ins292	GRCh37.p13	First Pass	NC_000007.13	Chr7	472,655	472,655

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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