A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602909



Internal ID16043632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35388863..35455712hg38UCSC Ensembl
Innerchr6:35356640..35423489hg19UCSC Ensembl
Innerchr6:35464618..35531467hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3866850
hg1966850
hg1866850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058198
Samples
Known GenesFANCE, PPARD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602909
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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