A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593411



Internal ID18891692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60326626..60431606hg38UCSC Ensembl
Innerchr3:60312356..60417339hg19UCSC Ensembl
Innerchr3:60287396..60392379hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38104981
hg19104984
hg18104984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013291
Supporting Variants
Samples
Known GenesFHIT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3593411
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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