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dbVar

Database of genomic structural variation

nsv5574797

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:89

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: 117 SVs from 28 studies. See in: genome view

Submitted genomic134,708,537-134,708,625

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5574797	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	134,708,537	134,708,625
nsv5574797	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	134,044,227	134,044,315

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17132136	deletion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17132136	Submitted genomic		NC_000005.10:g.134 708537_134708625de lG	GRCh38 (hg38)		NC_000005.10	Chr5	134,708,537	134,708,625
nssv17132136	Remapped	Perfect	NC_000005.9:g.1340 44227_134044315del G	GRCh37.p13	First Pass	NC_000005.9	Chr5	134,044,227	134,044,315

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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