A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576855



Internal ID16017578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:48549725..48615968hg38UCSC Ensembl
Innerchr18:46076096..46142339hg19UCSC Ensembl
Innerchr18:44330094..44396337hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3866244
hg1966244
hg1866244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150249
SamplesHGDP01235
Known GenesCTIF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576855
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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