A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053487



Internal ID15559987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31393708..31480538hg38UCSC Ensembl
Innerchr6:31361485..31448315hg19UCSC Ensembl
Innerchr6:31469464..31556294hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3886831
hg1986831
hg1886831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601911
Supporting Variants
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053487
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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