A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577059



Internal ID16364468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60276192..60307687hg38UCSC Ensembl
Innerchr18:57943425..57974920hg19UCSC Ensembl
Innerchr18:56094405..56125900hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3831496
hg1931496
hg1831496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv884915
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577059
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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