A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699876



Internal ID15089842
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524016
Supporting Variants
Samples
Known GenesKIAA1524
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699876
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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