A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593419



Internal ID18891700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60405824..60669469hg38UCSC Ensembl
Innerchr3:60391557..60655202hg19UCSC Ensembl
Innerchr3:60366597..60630242hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38263646
hg19263646
hg18263646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999284
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)nssv3593419
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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