A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829580



Internal ID15776850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:77829212..77830511hg38UCSC Ensembl
Innerchr14:78295555..78296854hg19UCSC Ensembl
Innerchr14:77365308..77366607hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381300
hg191300
hg181300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565223
Supporting Variants
Samples
Known GenesADCK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv829580
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer