A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053637



Internal ID15560137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31984717..31990466hg38UCSC Ensembl
Innerchr6:31952494..31958243hg19UCSC Ensembl
Innerchr6:32060473..32066222hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg385750
hg195750
hg185750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602004
Supporting Variants
Samples
Known GenesC4A, C4B, C4B_2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053637
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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