A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051850



Internal ID15558350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29889309..29941743hg38UCSC Ensembl
Innerchr6:29857086..29909520hg19UCSC Ensembl
Innerchr6:29965065..30017499hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3852435
hg1952435
hg1852435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601300
Supporting Variants
Samples
Known GenesHCG4B, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051850
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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