A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593755



Internal ID16381164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14214950..14479268hg38UCSC Ensembl
Innerchr4:14216574..14480892hg19UCSC Ensembl
Innerchr4:13825672..14089990hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38264319
hg19264319
hg18264319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv993080
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593755
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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