A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374260



Internal ID22599929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26658816..26661519hg38UCSC Ensembl
chr15:26903963..26906666hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg382704
hg192704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941594
Supporting Variants
Samples
Known GenesGABRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374260
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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