A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705885



Internal ID15442537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10195263..10236182hg38UCSC Ensembl
Innerchr3:10236947..10277866hg19UCSC Ensembl
Innerchr3:10211947..10252866hg18UCSC Ensembl
Innerchr3:10211947..10252866hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3840920
hg1940920
hg1840920
hg1740920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522516
Supporting Variants
Samples
Known GenesIRAK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705885
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