A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577908



Internal ID16018631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79739827..79767009hg38UCSC Ensembl
Innerchr18:77499827..77527009hg19UCSC Ensembl
Innerchr18:75600815..75627997hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3827183
hg1927183
hg1827183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6117n54
Supporting Variantsnssv890087, nssv890088
Samples
Known GenesCTDP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577908
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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