A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595517



Internal ID16382926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:135788675..136007297hg38UCSC Ensembl
Innerchr4:136709830..136928452hg19UCSC Ensembl
Innerchr4:136929280..137147902hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38218623
hg19218623
hg18218623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1007633
Samples
Known GenesLINC00613
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595517
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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