A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154299



Internal ID15534236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35489619..35534425hg38UCSC Ensembl
Innerchr6:35457396..35502202hg19UCSC Ensembl
Innerchr6:35565374..35610180hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3844807
hg1944807
hg1844807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602912
Supporting Variants
SamplesNINDS_49
Known GenesTEAD3, TULP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154299
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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