A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596023



Internal ID16036746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:163349101..163379624hg38UCSC Ensembl
Innerchr4:164270253..164300776hg19UCSC Ensembl
Innerchr4:164489703..164520226hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3830524
hg1930524
hg1830524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1010716
Samples
Known GenesNPY5R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596023
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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