A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593754



Internal ID16381163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:13495261..13540412hg38UCSC Ensembl
Innerchr4:13496885..13542036hg19UCSC Ensembl
Innerchr4:13105983..13151134hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3845152
hg1945152
hg1845152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv993079
Samples
Known GenesLINC01097
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593754
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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