A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579869



Internal ID16020592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45356868..45365051hg38UCSC Ensembl
Innerchr19:45860126..45868309hg19UCSC Ensembl
Innerchr19:50551966..50560149hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg388184
hg198184
hg188184
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899936
Samples
Known GenesERCC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579869
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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