A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593898



Internal ID16381307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:30346431..30656913hg38UCSC Ensembl
Innerchr4:30348053..30658535hg19UCSC Ensembl
Innerchr4:29957151..30267633hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38310483
hg19310483
hg18310483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152599
Samples1780862250_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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