A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1050625



Internal ID15903811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:18984068..19034180hg38UCSC Ensembl
Innerchr6:18984299..19034411hg19UCSC Ensembl
Innerchr6:19092278..19142390hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3850113
hg1950113
hg1850113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601061
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1050625
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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