A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv886482



Internal ID16180438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68983651..69039618hg38UCSC Ensembl
Innerchr18:66650888..66706855hg19UCSC Ensembl
Innerchr18:64801868..64857835hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3855968
hg1955968
hg1855968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577375
Supporting Variants
Samples
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv886482
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