A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv889149



Internal ID15836419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79516964..79530026hg38UCSC Ensembl
Innerchr18:77276964..77290026hg19UCSC Ensembl
Innerchr18:75377952..75391014hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3813063
hg1913063
hg1813063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577885
Supporting Variants
Samples
Known GenesNFATC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv889149
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