A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051649



Internal ID15904835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27687785..27721723hg38UCSC Ensembl
Innerchr6:27655564..27689502hg19UCSC Ensembl
Innerchr6:27763543..27797481hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3833939
hg1933939
hg1833939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601204
Supporting Variants
Samples
Known GenesLINC01012
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051649
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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