A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520012



Internal ID15100619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136369196..136595277hg38UCSC Ensembl
Innerchr3:136088038..136314119hg19UCSC Ensembl
Innerchr3:137570728..137796809hg18UCSC Ensembl
Innerchr3:137570736..137796817hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38226082
hg19226082
hg18226082
hg17226082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682203, nssv660078
Samples
Known GenesSTAG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520012
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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