A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009465



Internal ID19098683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62685607..62709238hg38UCSC Ensembl
Innerchr3:62671282..62694913hg19UCSC Ensembl
Innerchr3:62646322..62669953hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3823632
hg1923632
hg1823632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4756n100
Supporting Variantsnssv3594562, nssv3594563, nssv3594564, nssv3594560, nssv3594561
Samples
Known GenesCADPS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009465
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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