A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524016



Internal ID15104623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108566875..108589473hg38UCSC Ensembl
Innerchr3:108285722..108308320hg19UCSC Ensembl
Innerchr3:109768412..109791010hg18UCSC Ensembl
Innerchr3:109768412..109791010hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3822599
hg1922599
hg1822599
hg1722599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699876
Samples
Known GenesKIAA1524
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524016
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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