A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053779



Internal ID15560279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31996100..32042495hg38UCSC Ensembl
Innerchr6:31963877..32010272hg19UCSC Ensembl
Innerchr6:32071855..32118251hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3846396
hg1946396
hg1846397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602043
Supporting Variants
Samples
Known GenesC4A, C4B, C4B_2, CYP21A1P, CYP21A2, STK19, TNXA, TNXB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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