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dbVar

Database of genomic structural variation

nsv5615464

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

Submitted genomic100,436,923-100,436,923

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5615464	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	100,436,923	100,436,923
nsv5615464	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	100,155,767	100,155,767

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17129488	insertion	SAMN00000419	Sequencing	Sequence alignment	1,071

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17129488	Submitted genomic		NC_000003.12:g.100 436923_100436924in s341	GRCh38 (hg38)		NC_000003.12	Chr3	100,436,923	100,436,923
nssv17129488	Remapped	Perfect	NC_000003.11:g.100 155767_100155768in s341	GRCh37.p13	First Pass	NC_000003.11	Chr3	100,155,767	100,155,767

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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