A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055462



Internal ID19144681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29384930..29441192hg38UCSC Ensembl
Innerchr19:29875837..29932099hg19UCSC Ensembl
Innerchr19:34567677..34623939hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3856263
hg1956263
hg1856263
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566529
Samples
Known GenesLOC284395
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055462
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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