A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602110



Internal ID16042833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32387906..32394044hg38UCSC Ensembl
Innerchr6:32355683..32361821hg19UCSC Ensembl
Innerchr6:32463661..32469799hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg386139
hg196139
hg186139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1053912
Samples
Known GenesHCG23
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602110
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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