A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1059617



Internal ID15566117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:54021120..54238996hg38UCSC Ensembl
Innerchr6:53885918..54103794hg19UCSC Ensembl
Innerchr6:53993877..54211753hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38217877
hg19217877
hg18217877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603110
Supporting Variants
Samples
Known GenesMLIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1059617
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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