A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593783



Internal ID16381192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19052136..19111323hg38UCSC Ensembl
Innerchr4:19053759..19112946hg19UCSC Ensembl
Innerchr4:18662857..18722044hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3859188
hg1959188
hg1859188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv993116
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593783
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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