A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701125



Internal ID15091091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:105286009..105690477hg38UCSC Ensembl
Innerchr3:105004853..105409321hg19UCSC Ensembl
Innerchr3:106487543..106892011hg18UCSC Ensembl
Innerchr3:106487543..106892011hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38404469
hg19404469
hg18404469
hg17404469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525071
Supporting Variants
Samples
Known GenesALCAM, CBLB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701125
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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