A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578689



Internal ID16366098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14934418..14937995hg38UCSC Ensembl
Innerchr19:15045230..15048807hg19UCSC Ensembl
Innerchr19:14906230..14909807hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383578
hg193578
hg183578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6283n54
Supporting Variantsnssv894939
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578689
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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