A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1052350



Internal ID15905536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31269628..31342279hg38UCSC Ensembl
Innerchr6:31237405..31310056hg19UCSC Ensembl
Innerchr6:31345384..31418035hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3872652
hg1972652
hg1872652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601506
Supporting Variants
Samples
Known GenesHLA-C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1052350
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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