A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578152



Internal ID16365561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:572860..583812hg38UCSC Ensembl
Innerchr19:572860..583812hg19UCSC Ensembl
Innerchr19:523860..534812hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810953
hg1910953
hg1810953
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891222
Samples
Known GenesBSG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578152
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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