A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526874



Internal ID15454167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:138056019..138073250hg38UCSC Ensembl
Innerchr4:138977173..138994404hg19UCSC Ensembl
Innerchr4:139196623..139213854hg18UCSC Ensembl
Innerchr4:139334778..139352009hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3817232
hg1917232
hg1817232
hg1717232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703232
Samples
Known GenesLINC00616
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526874
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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