A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595580



Internal ID16036303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:138045351..138051121hg38UCSC Ensembl
Innerchr4:138966505..138972275hg19UCSC Ensembl
Innerchr4:139185955..139191725hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg385771
hg195771
hg185771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1008208
Samples
Known GenesLINC00616
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595580
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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