A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602959



Internal ID16390368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:38760366..38818752hg38UCSC Ensembl
Innerchr6:38728142..38786528hg19UCSC Ensembl
Innerchr6:38836120..38894506hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3858387
hg1958387
hg1858387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154305
SamplesHGDP00914
Known GenesDNAH8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602959
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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