A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516380



Internal ID15096987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62679605..62710892hg38UCSC Ensembl
Innerchr3:62665280..62696567hg19UCSC Ensembl
Innerchr3:62640320..62671607hg18UCSC Ensembl
Innerchr3:62640320..62671607hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3831288
hg1931288
hg1831288
hg1731288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667919, nssv681168, nssv686934, nssv678077, nssv678014, nssv686112, nssv672741, nssv692876, nssv676118
Samples
Known GenesCADPS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516380
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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