A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060207



Internal ID19149426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32086518..32110647hg38UCSC Ensembl
Innerchr19:32577424..32601553hg19UCSC Ensembl
Innerchr19:37269264..37293393hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3824130
hg1924130
hg1824130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3724353
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)nsv1060207
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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