A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593315



Internal ID16034038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1526039..1594238hg38UCSC Ensembl
Innerchr4:1527766..1595965hg19UCSC Ensembl
Innerchr4:1498513..1565924hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3868200
hg1968200
hg1867412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8895n54
Supporting Variantsnssv987705
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593315
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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