A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576429



Internal ID16363838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8417486..8471459hg38UCSC Ensembl
Innerchr18:8417484..8471457hg19UCSC Ensembl
Innerchr18:8407484..8461457hg18UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg3853974
hg1953974
hg1853974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878028
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576429
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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