A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579517



Internal ID16366926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39894797..39895316hg38UCSC Ensembl
Innerchr19:40385437..40385956hg19UCSC Ensembl
Innerchr19:45077277..45077796hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38520
hg19520
hg18520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6441n54
Supporting Variantsnssv899270, nssv899269
Samples
Known GenesFCGBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579517
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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