A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695378



Internal ID15085344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73057292..73196412hg38UCSC Ensembl
Innerchr15:73349633..73488753hg19UCSC Ensembl
Innerchr15:71136686..71275806hg18UCSC Ensembl
Innerchr15:71136686..71275806hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38139121
hg19139121
hg18139121
hg17139121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517966
Supporting Variants
Samples
Known GenesNEO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695378
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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