A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593407



Internal ID18891688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60276888..60358458hg38UCSC Ensembl
Innerchr3:60262617..60344190hg19UCSC Ensembl
Innerchr3:60237657..60319230hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3881571
hg1981574
hg1881574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001134
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)nssv3593407
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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