A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520875



Internal ID15448168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:139929484..139930821hg38UCSC Ensembl
Innerchr3:139648326..139649663hg19UCSC Ensembl
Innerchr3:141131016..141132353hg18UCSC Ensembl
Innerchr3:141131024..141132361hg17UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381338
hg191338
hg181338
hg171338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694405
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520875
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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