A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579282



Internal ID16020005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29960594..30000137hg38UCSC Ensembl
Innerchr19:30451501..30491044hg19UCSC Ensembl
Innerchr19:35143341..35182884hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3839544
hg1939544
hg1839544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv897585
Samples
Known GenesURI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579282
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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