A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589564



Internal ID18887845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:27025693..27064874hg38UCSC Ensembl
Innerchr3:27067184..27106365hg19UCSC Ensembl
Innerchr3:27042188..27081369hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3839182
hg1939182
hg1839182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005432
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589564
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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