A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704933



Internal ID15094899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138306554..138413551hg38UCSC Ensembl
Innerchr3:138025396..138132393hg19UCSC Ensembl
Innerchr3:139508086..139615083hg18UCSC Ensembl
Innerchr3:139508094..139615091hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38106998
hg19106998
hg18106998
hg17106998
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528349
Supporting Variants
Samples
Known GenesMRAS, NME9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704933
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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