A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687400



Internal ID15424052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85748317..85766789hg38UCSC Ensembl
Innerchr15:86291548..86310020hg19UCSC Ensembl
Innerchr15:84092552..84111024hg18UCSC Ensembl
Innerchr15:84092552..84111024hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3818473
hg1918473
hg1818473
hg1718473
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516322
Supporting Variants
Samples
Known GenesAKAP13, KLHL25
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687400
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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