A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1058392



Internal ID15911578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:38939426..38972506hg38UCSC Ensembl
Innerchr6:38907202..38940282hg19UCSC Ensembl
Innerchr6:39015180..39048260hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3833081
hg1933081
hg1833081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602962
Supporting Variants
Samples
Known GenesDNAH8, LOC100131047
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1058392
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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