A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528045



Internal ID15108652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:168527477..168533166hg38UCSC Ensembl
Innerchr4:169448628..169454317hg19UCSC Ensembl
Innerchr4:169685203..169690892hg18UCSC Ensembl
Innerchr4:169823358..169829047hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg385690
hg195690
hg185690
hg175690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704577
Samples
Known GenesPALLD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528045
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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