A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696171



Internal ID15086137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30054027..30814623hg38UCSC Ensembl
Innerchr15:30346230..31106826hg19UCSC Ensembl
Innerchr15:28133522..28894118hg18UCSC Ensembl
Innerchr15:28133522..28894118hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38760597
hg19760597
hg18760597
hg17760597
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518720
Supporting Variants
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC100288637, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696171
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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