A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688804



Internal ID15078770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126496558..126508098hg38UCSC Ensembl
Innerchr9:129258837..129270377hg19UCSC Ensembl
Innerchr9:128298658..128310198hg18UCSC Ensembl
Innerchr9:126338391..126349931hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3811541
hg1911541
hg1811541
hg1711541
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516074
Supporting Variants
Samples
Known GenesMVB12B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688804
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