A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518644



Internal ID15445937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39707188..39726889hg38UCSC Ensembl
Innerchr4:39708808..39728509hg19UCSC Ensembl
Innerchr4:39385203..39404904hg18UCSC Ensembl
Innerchr4:39531374..39551075hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3819702
hg1919702
hg1819702
hg1719702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696093
Samples
Known GenesUBE2K
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518644
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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