A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153717



Internal ID15874611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65926311..66009704hg38UCSC Ensembl
Innerchr6:66636204..66719597hg19UCSC Ensembl
Innerchr6:66692925..66776318hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3883394
hg1983394
hg1883394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603476
Supporting Variants
SamplesHGDP00562
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153717
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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