A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664756



Internal ID15054722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34355367..34508394hg38UCSC Ensembl
Innerchr15:34647568..34800595hg19UCSC Ensembl
Innerchr15:32434860..32587887hg18UCSC Ensembl
Innerchr15:32434860..32587887hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38153028
hg19153028
hg18153028
hg17153028
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517751
Supporting Variants
Samples
Known GenesGOLGA8A, LPCAT4, MIR1233-1, MIR1233-2, NUTM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664756
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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