A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053638



Internal ID15560138
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 gain
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)nssv1053638
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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