A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601167



Internal ID16388576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:25155969..25234656hg38UCSC Ensembl
Innerchr6:25156197..25234884hg19UCSC Ensembl
Innerchr6:25264176..25342863hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3878688
hg1978688
hg1878688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154035
Samples1780862224_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601167
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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