A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689350



Internal ID15079316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135714078..135752357hg38UCSC Ensembl
Innerchr9:138605924..138644203hg19UCSC Ensembl
Innerchr9:137745745..137784024hg18UCSC Ensembl
Innerchr9:135831869..135870148hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3838280
hg1938280
hg1838280
hg1738280
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)nssv689350
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