A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697365



Internal ID15434017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113637872..113643195hg38UCSC Ensembl
Innerchr9:116400152..116405475hg19UCSC Ensembl
Innerchr9:115439973..115445296hg18UCSC Ensembl
Innerchr9:113479706..113485029hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg385324
hg195324
hg185324
hg175324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516235
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697365
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