A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602107



Internal ID16042830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32188959..32193653hg38UCSC Ensembl
Innerchr6:32156736..32161430hg19UCSC Ensembl
Innerchr6:32264714..32269408hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384695
hg194695
hg184695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10486n54
Supporting Variantsnssv1053908, nssv1053907
Samples
Known GenesGPSM3, PBX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602107
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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