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dbVar

Database of genomic structural variation

nsv5632078

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

Submitted genomic124,711,536-124,711,536

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5632078	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	124,711,536	124,711,536
nsv5632078	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	125,723,777	125,723,777

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17155899	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
nssv17155899	Submitted genomic		NC_000008.11:g.124 711536_124711537in s104	GRCh38 (hg38)		NC_000008.11	Chr8	124,711,536	124,711,536
nssv17155899	Remapped	Perfect	NC_000008.10:g.125 723777_125723778in s104	GRCh37.p13	First Pass	NC_000008.10	Chr8	125,723,777	125,723,777

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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