A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576476



Internal ID16017199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10487446..10515297hg38UCSC Ensembl
Innerchr18:10487443..10515294hg19UCSC Ensembl
Innerchr18:10477443..10505294hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3827852
hg1927852
hg1827852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150590
SamplesHGDP01372
Known GenesAPCDD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576476
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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