A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656778



Internal ID15393430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85748317..85797294hg38UCSC Ensembl
Innerchr15:86291548..86340525hg19UCSC Ensembl
Innerchr15:84092552..84141529hg18UCSC Ensembl
Innerchr15:84092552..84141529hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3848978
hg1948978
hg1848978
hg1748978
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)nssv656778
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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