A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667566



Internal ID15404218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85745036..85797294hg38UCSC Ensembl
Innerchr15:86288267..86340525hg19UCSC Ensembl
Innerchr15:84089271..84141529hg18UCSC Ensembl
Innerchr15:84089271..84141529hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3852259
hg1952259
hg1852259
hg1752259
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)nssv667566
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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