A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1010716



Internal ID15957986
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 StatusS
Merged Variantsnsv596023
Supporting Variants
Samples
Known GenesNPY5R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1010716
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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