A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605186



Internal ID16392595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162940164..163011332hg38UCSC Ensembl
Innerchr6:163361196..163432364hg19UCSC Ensembl
Innerchr6:163281186..163352354hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3871169
hg1971169
hg1871169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154698
SamplesHGDP00251
Known GenesPACRG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605186
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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