A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525389



Internal ID15105996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:40005664..40046132hg38UCSC Ensembl
Innerchr4:40007284..40047752hg19UCSC Ensembl
Innerchr4:39683679..39724147hg18UCSC Ensembl
Innerchr4:39829850..39870318hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3840469
hg1940469
hg1840469
hg1740469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701511
Samples
Known GenesLOC344967
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525389
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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