A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611137



Internal ID21803184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85513776..85515967hg38UCSC Ensembl
chr15:86057007..86059198hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg382192
hg192192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031017
Supporting Variants
Samples
Known GenesAKAP13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611137
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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