A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568244



Internal ID16008967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22567965..23094188hg38UCSC Ensembl
Innerchr15:22778880..23305131hg19UCSC Ensembl
Innerchr15:20330244..20856572hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38526224
hg19526252
hg18526329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4318n54
Supporting Variantsnssv838367
Samples
Known GenesCYFIP1, GOLGA8I, HERC2P2, LOC283683, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568244
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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