A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576575



Internal ID16363984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:25920509..25982555hg38UCSC Ensembl
Innerchr18:23500473..23562519hg19UCSC Ensembl
Innerchr18:21754471..21816517hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3862047
hg1962047
hg1862047
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878498
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576575
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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