A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577655



Internal ID16365064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74463196..74504009hg38UCSC Ensembl
Innerchr18:72130431..72171244hg19UCSC Ensembl
Innerchr18:70281411..70322224hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3840814
hg1940814
hg1840814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887380
Samples
Known GenesCNDP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577655
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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