A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579910



Internal ID16367319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:49915478..49957657hg38UCSC Ensembl
Innerchr19:50418735..50460914hg19UCSC Ensembl
Innerchr19:55110547..55152726hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3842180
hg1942180
hg1842180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150654
SamplesNINDS_67
Known GenesATF5, IL4I1, MIR4751, NUP62, SIGLEC11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579910
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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