A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576551



Internal ID16363960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15108541..15229052hg38UCSC Ensembl
Innerchr18:15108540..15229051hg19UCSC Ensembl
Innerchr18:15098540..15219051hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38120512
hg19120512
hg18120512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878474, nssv878475
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576551
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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