A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602065



Internal ID16042788
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 StatusM
Merged Variantsdgv10476n54
Supporting Variantsnssv1053807, nssv1053808, nssv1053809
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)nsv602065
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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