A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1052003



Internal ID15558503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29893749..29931370hg38UCSC Ensembl
Innerchr6:29861526..29899147hg19UCSC Ensembl
Innerchr6:29969505..30007126hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3837622
hg1937622
hg1837622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601352
Supporting Variants
Samples
Known GenesHCG4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1052003
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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