A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012890



Internal ID19102107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162160292..162235401hg38UCSC Ensembl
Innerchr3:161878080..161953189hg19UCSC Ensembl
Innerchr3:163360774..163435883hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3875110
hg1975110
hg1875110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4932n100
Supporting Variantsnssv3607932
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)nsv1012890
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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