A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv886384



Internal ID15833654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67481097..67552997hg38UCSC Ensembl
Innerchr18:65148334..65220234hg19UCSC Ensembl
Innerchr18:63299314..63371214hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3871901
hg1971901
hg1871901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577312
Supporting Variants
Samples
Known GenesDSEL, LOC643542
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv886384
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