A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963402



Internal ID16257358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60325060..60431370hg38UCSC Ensembl
Innerchr3:60310790..60417103hg19UCSC Ensembl
Innerchr3:60285830..60392143hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38106311
hg19106314
hg18106314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590395
Supporting Variants
Samples
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963402
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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