A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694615



Internal ID15084581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30848497..30980467hg38UCSC Ensembl
Innerchr15:31140700..31272670hg19UCSC Ensembl
Innerchr15:28927992..29059962hg18UCSC Ensembl
Innerchr15:28927992..29059962hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38131971
hg19131971
hg18131971
hg17131971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521842
Supporting Variants
Samples
Known GenesFAN1, MIR7976, MTMR10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694615
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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