A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008267



Internal ID19097486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60086221..60278732hg38UCSC Ensembl
Innerchr3:60071947..60264461hg19UCSC Ensembl
Innerchr3:60046987..60239501hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38192512
hg19192515
hg18192515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4750n100
Supporting Variantsnssv3593404
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)nsv1008267
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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