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dbVar

Database of genomic structural variation

nsv5619394

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: 96 SVs from 26 studies. See in: genome view

Submitted genomic101,560,799-101,560,799

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5619394	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	101,560,799	101,560,799
nsv5619394	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	101,279,643	101,279,643

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17125413	insertion	SAMN00801888	Sequencing	Sequence alignment	2,004

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17125413	Submitted genomic		NC_000003.12:g.101 560799_101560800in s6069	GRCh38 (hg38)		NC_000003.12	Chr3	101,560,799	101,560,799
nssv17125413	Remapped	Perfect	NC_000003.11:g.101 279643_101279644in s6069	GRCh37.p13	First Pass	NC_000003.11	Chr3	101,279,643	101,279,643

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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