A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv960155



Internal ID16254111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26383758..26397924hg38UCSC Ensembl
Innerchr3:26425249..26439415hg19UCSC Ensembl
Innerchr3:26400253..26414419hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3814167
hg1914167
hg1814167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589971
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)nssv960155
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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