A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053809



Internal ID15560309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32009677..32029164hg38UCSC Ensembl
Innerchr6:31977454..31996941hg19UCSC Ensembl
Innerchr6:32085432..32104919hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3819488
hg1919488
hg1819488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602065
Supporting Variants
Samples
Known GenesC4A, C4B, C4B_2, STK19, TNXA, TNXB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053809
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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