A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601872



Internal ID16042595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31387541..31475546hg38UCSC Ensembl
Innerchr6:31355318..31443323hg19UCSC Ensembl
Innerchr6:31463297..31551302hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3888006
hg1988006
hg1888006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10453n54
Supporting Variantsnssv1154253
SamplesHGDP01023
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601872
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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