A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1072356



Internal ID15925542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:120103739..120188045hg38UCSC Ensembl
Innerchr6:120424885..120509191hg19UCSC Ensembl
Innerchr6:120466584..120550890hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3884307
hg1984307
hg1884307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604566
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)nssv1072356
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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