A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601888



Internal ID16042611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31391416..31486588hg38UCSC Ensembl
Innerchr6:31359193..31454365hg19UCSC Ensembl
Innerchr6:31467172..31562344hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3895173
hg1995173
hg1895173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10454n54
Supporting Variantsnssv1053415, nssv1053414
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601888
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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