A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576650



Internal ID16364059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:34284257..34391122hg38UCSC Ensembl
Innerchr18:31864221..31971086hg19UCSC Ensembl
Innerchr18:30118219..30225084hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38106866
hg19106866
hg18106866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878960
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576650
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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