A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579632



Internal ID16020355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42400501..42408251hg38UCSC Ensembl
Innerchr19:42904653..42912403hg19UCSC Ensembl
Innerchr19:47596493..47604243hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg387751
hg197751
hg187751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899604
Samples
Known GenesLIPE, LIPE-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579632
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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