A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524090



Internal ID15451383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28589633..28603787hg38UCSC Ensembl
Innerchr3:28631124..28645278hg19UCSC Ensembl
Innerchr3:28606128..28620282hg18UCSC Ensembl
Innerchr3:28606128..28620282hg17UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3814155
hg1914155
hg1814155
hg1714155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699962
Samples
Known GenesLINC00693
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524090
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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