A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577907



Internal ID16018630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79739827..79766471hg38UCSC Ensembl
Innerchr18:77499827..77526471hg19UCSC Ensembl
Innerchr18:75600815..75627459hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3826645
hg1926645
hg1826645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6117n54
Supporting Variantsnssv890084, nssv890085, nssv890086, nssv890083
Samples
Known GenesCTDP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577907
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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