A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004959



Internal ID19094176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11883204..11910532hg38UCSC Ensembl
Innerchr3:11924678..11952006hg19UCSC Ensembl
Innerchr3:11899678..11927006hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3827329
hg1927329
hg1827329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4682n100
Supporting Variantsnssv3591944, nssv3591946, nssv3591947, nssv3591945, nssv3591948
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)nsv1004959
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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