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dbVar

Database of genomic structural variation

nsv5613822

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: 166 SVs from 33 studies. See in: genome view

Submitted genomic113,015,584-113,015,584

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5613822	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	113,015,584	113,015,584
nsv5613822	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	112,734,431	112,734,431

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17122529	insertion	SAMN00006466	Sequencing	Sequence alignment	4,625

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17122529	Submitted genomic		NC_000003.12:g.113 015584_113015585in s311	GRCh38 (hg38)		NC_000003.12	Chr3	113,015,584	113,015,584
nssv17122529	Remapped	Perfect	NC_000003.11:g.112 734431_112734432in s311	GRCh37.p13	First Pass	NC_000003.11	Chr3	112,734,431	112,734,431

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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