A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576552



Internal ID16363961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15178341..15290107hg38UCSC Ensembl
Innerchr18:15178340..15290106hg19UCSC Ensembl
Innerchr18:15168340..15280106hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38111767
hg19111767
hg18111767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5869n54
Supporting Variantsnssv878476
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576552
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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