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dbVar

Database of genomic structural variation

nsv5638242

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: 249 SVs from 42 studies. See in: genome view

Submitted genomic1,059,664-1,059,664

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5638242	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	1,059,664	1,059,664
nsv5638242	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	1,099,300	1,099,300

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17140181	insertion	SAMN00000485	Sequencing	Sequence alignment	1,404

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17140181	Submitted genomic		NC_000007.14:g.105 9664_1059665ins148	GRCh38 (hg38)		NC_000007.14	Chr7	1,059,664	1,059,664
nssv17140181	Remapped	Perfect	NC_000007.13:g.109 9300_1099301ins148	GRCh37.p13	First Pass	NC_000007.13	Chr7	1,099,300	1,099,300

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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