A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516520



Internal ID15443813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18948864..18954865hg38UCSC Ensembl
Innerchr3:18990356..18996357hg19UCSC Ensembl
Innerchr3:18965360..18971361hg18UCSC Ensembl
Innerchr3:18965360..18971361hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg386002
hg196002
hg186002
hg176002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671551, nssv668818, nssv687331
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516520
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer