A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1069239



Internal ID15922425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:95433859..95500984hg38UCSC Ensembl
Innerchr6:95881735..95948860hg19UCSC Ensembl
Innerchr6:95988456..96055581hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3867126
hg1967126
hg1867126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604237
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)nssv1069239
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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