A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528320



Internal ID15455613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:164888162..164906597hg38UCSC Ensembl
Innerchr4:165809314..165827749hg19UCSC Ensembl
Innerchr4:166028764..166047199hg18UCSC Ensembl
Innerchr4:166166919..166185354hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3818436
hg1918436
hg1818436
hg1718436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704901
Samples
Known GenesLOC100506013
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528320
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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