A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593897



Internal ID16381306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:30081723..30320320hg38UCSC Ensembl
Innerchr4:30083345..30321942hg19UCSC Ensembl
Innerchr4:29692443..29931040hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38238598
hg19238598
hg18238598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv995197, nssv995196
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593897
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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