A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3731128



Internal ID19029409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60082140..60291399hg38UCSC Ensembl
Innerchr3:60067866..60277128hg19UCSC Ensembl
Innerchr3:60042906..60252168hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38209260
hg19209263
hg18209263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009063
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)nssv3731128
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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