A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602903



Internal ID16390312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34448611..34525235hg38UCSC Ensembl
Innerchr6:34416388..34493012hg19UCSC Ensembl
Innerchr6:34524366..34600990hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3876625
hg1976625
hg1876625
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154296
SamplesHGDP01211
Known GenesPACSIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602903
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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