A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595579



Internal ID16036302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:138045351..138047403hg38UCSC Ensembl
Innerchr4:138966505..138968557hg19UCSC Ensembl
Innerchr4:139185955..139188007hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg382053
hg192053
hg182053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1008207
Samples
Known GenesLINC00616
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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