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dbVar

Database of genomic structural variation

nsv5645894

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

Submitted genomic56,739,894-56,739,894

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5645894	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	56,739,894	56,739,894
nsv5645894	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	56,773,806	56,773,806

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17096475	insertion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17096475	Submitted genomic		NC_000016.10:g.567 39894_56739895ins2 78	GRCh38 (hg38)		NC_000016.10	Chr16	56,739,894	56,739,894
nssv17096475	Remapped	Perfect	NC_000016.9:g.5677 3806_56773807ins27 8	GRCh37.p13	First Pass	NC_000016.9	Chr16	56,773,806	56,773,806

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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