A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv879927



Internal ID16173883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39656488..39921823hg38UCSC Ensembl
Innerchr18:37236452..37501787hg19UCSC Ensembl
Innerchr18:35490450..35755785hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38265336
hg19265336
hg18265336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576671
Supporting Variants
Samples
Known GenesLINC00669, MIR5583-1, MIR5583-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv879927
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