A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv888882



Internal ID16182838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78979558..78980976hg38UCSC Ensembl
Innerchr18:76739558..76740976hg19UCSC Ensembl
Innerchr18:74840546..74841964hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381419
hg191419
hg181419
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577811
Supporting Variants
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv888882
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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