A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv884939



Internal ID15832209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:61275224..61335721hg38UCSC Ensembl
Innerchr18:58942457..59002954hg19UCSC Ensembl
Innerchr18:57093437..57153934hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3860498
hg1960498
hg1860498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577074
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)nssv884939
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