A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524965



Internal ID15452258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2285694..2295823hg38UCSC Ensembl
Innerchr4:2287421..2297550hg19UCSC Ensembl
Innerchr4:2257219..2267348hg18UCSC Ensembl
Innerchr4:2254652..2264781hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3810130
hg1910130
hg1810130
hg1710130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700987
Samples
Known GenesZFYVE28
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524965
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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