A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697636



Internal ID15434288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85748317..85786279hg38UCSC Ensembl
Innerchr15:86291548..86329510hg19UCSC Ensembl
Innerchr15:84092552..84130514hg18UCSC Ensembl
Innerchr15:84092552..84130514hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3837963
hg1937963
hg1837963
hg1737963
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516322
Supporting Variants
Samples
Known GenesAKAP13, KLHL25, MIR1276
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697636
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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