A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577371



Internal ID16364780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68928378..69044336hg38UCSC Ensembl
Innerchr18:66595615..66711573hg19UCSC Ensembl
Innerchr18:64746595..64862553hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38115959
hg19115959
hg18115959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv886478
Samples
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577371
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