A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601702



Internal ID16389111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31316567..31357843hg38UCSC Ensembl
Innerchr6:31284344..31325620hg19UCSC Ensembl
Innerchr6:31392323..31433599hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3841277
hg1941277
hg1841277
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10381n54
Supporting Variantsnssv1053072
Samples
Known GenesHLA-B, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601702
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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