A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525527



Internal ID15452820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:115682594..116297321hg38UCSC Ensembl
Innerchr4:116603750..117218477hg19UCSC Ensembl
Innerchr4:116823199..117437926hg18UCSC Ensembl
Innerchr4:116961354..117576081hg17UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38614728
hg19614728
hg18614728
hg17614728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701662
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525527
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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