A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518493



Internal ID15099100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149537528..149540279hg38UCSC Ensembl
Innerchr3:149255315..149258066hg19UCSC Ensembl
Innerchr3:150738005..150740756hg18UCSC Ensembl
Innerchr3:150738013..150740764hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382752
hg192752
hg182752
hg172752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695933
Samples
Known GenesWWTR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518493
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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