A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv885139



Internal ID15832409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:65608005..65715200hg38UCSC Ensembl
Innerchr18:63275241..63382436hg19UCSC Ensembl
Innerchr18:61426221..61533416hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38107196
hg19107196
hg18107196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577155
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv885139
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