A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690229



Internal ID15080195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135711894..135739808hg38UCSC Ensembl
Innerchr9:138603740..138631654hg19UCSC Ensembl
Innerchr9:137743561..137771475hg18UCSC Ensembl
Innerchr9:135829685..135857599hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3827915
hg1927915
hg1827915
hg1727915
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517335
Supporting Variants
Samples
Known GenesKCNT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690229
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