A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv886492



Internal ID16180448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69016897..69082913hg38UCSC Ensembl
Innerchr18:66684134..66750150hg19UCSC Ensembl
Innerchr18:64835114..64901130hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3866017
hg1966017
hg1866017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577384
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)nssv886492
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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