A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602991



Internal ID16043714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42089587..42131633hg38UCSC Ensembl
Innerchr6:42057325..42099371hg19UCSC Ensembl
Innerchr6:42165303..42207349hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3842047
hg1942047
hg1842047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10639n54
Supporting Variantsnssv1153693
SamplesNINDS_65
Known GenesC6orf132
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602991
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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