A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577329



Internal ID16018052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68025058..68867575hg38UCSC Ensembl
Innerchr18:65692295..66534812hg19UCSC Ensembl
Innerchr18:63843275..64685792hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38842518
hg19842518
hg18842518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150257
Samples1780854159_A
Known GenesCCDC102B, TMX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577329
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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