A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579850



Internal ID16367259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43380933..43455962hg38UCSC Ensembl
Innerchr19:43885085..43960114hg19UCSC Ensembl
Innerchr19:48576925..48651954hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3875030
hg1975030
hg1875030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899915
Samples
Known GenesTEX101
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579850
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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