A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593791



Internal ID16034514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:20260163..20290616hg38UCSC Ensembl
Innerchr4:20261786..20292239hg19UCSC Ensembl
Innerchr4:19870884..19901337hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3830454
hg1930454
hg1830454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152885
Samples1780862042_A
Known GenesSLIT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593791
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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