A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521842



Internal ID15102449
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 StatusM
Merged Variants
Supporting Variantsnssv694615
Samples
Known GenesFAN1, MIR7976, MTMR10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521842
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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