A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593893



Internal ID16381302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28590532..28659904hg38UCSC Ensembl
Innerchr4:28592154..28661526hg19UCSC Ensembl
Innerchr4:28201252..28270624hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3869373
hg1969373
hg1869373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152598
Samples1780862109_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593893
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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