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dbVar

Database of genomic structural variation

nsv5664443

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: 95 SVs from 20 studies. See in: genome view

Submitted genomic96,415,728-96,415,728

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5664443	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	96,415,728	96,415,728
nsv5664443	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	96,882,065	96,882,065

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17098798	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17098798	Submitted genomic		NC_000014.9:g.9641 5728_96415729ins10 5	GRCh38 (hg38)		NC_000014.9	Chr14	96,415,728	96,415,728
nssv17098798	Remapped	Perfect	NC_000014.8:g.9688 2065_96882066ins10 5	GRCh37.p13	First Pass	NC_000014.8	Chr14	96,882,065	96,882,065

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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