A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997531



Internal ID19157067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60354708..60519259hg38UCSC Ensembl
Innerchr3:60340440..60504992hg19UCSC Ensembl
Innerchr3:60315480..60480032hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38164552
hg19164553
hg18164553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593412
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)nsv997531
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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