A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601878



Internal ID16042601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31387541..31485841hg38UCSC Ensembl
Innerchr6:31355318..31453618hg19UCSC Ensembl
Innerchr6:31463297..31561597hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3898301
hg1998301
hg1898301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10453n54
Supporting Variantsnssv1053400
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)nsv601878
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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