A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154100



Internal ID15879134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77374254..77417657hg38UCSC Ensembl
Innerchr6:78083971..78127374hg19UCSC Ensembl
Innerchr6:78140690..78184093hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3843404
hg1943404
hg1843404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603809
Supporting Variants
SamplesHGDP01312
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154100
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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