A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702527



Internal ID15092493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77974844..78001610hg38UCSC Ensembl
Innerchr9:80589760..80616526hg19UCSC Ensembl
Innerchr9:79779580..79806346hg18UCSC Ensembl
Innerchr9:77819314..77846080hg17UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3826767
hg1926767
hg1826767
hg1726767
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526255
Supporting Variants
Samples
Known GenesGNAQ
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702527
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