A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153624



Internal ID15874762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:8943955..9140425hg38UCSC Ensembl
Innerchr6:8944188..9140658hg19UCSC Ensembl
Innerchr6:8889187..9085657hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38196471
hg19196471
hg18196471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600964
Supporting Variants
SamplesHGDP00585
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153624
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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