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dbVar

Database of genomic structural variation

nsv5671894

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: 239 SVs from 29 studies. See in: genome view

Submitted genomic31,947,172-31,947,172

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5671894	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	31,947,172	31,947,172
nsv5671894	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	33,319,484	33,319,484

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17119062	insertion	HG03486	Sequencing	Sequence alignment	4,355

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17119062	Submitted genomic		NC_000021.9:g.3194 7172_31947173ins77	GRCh38 (hg38)		NC_000021.9	Chr21	31,947,172	31,947,172
nssv17119062	Remapped	Perfect	NC_000021.8:g.3331 9484_33319485ins77	GRCh37.p13	First Pass	NC_000021.8	Chr21	33,319,484	33,319,484

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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