A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577608



Internal ID16365017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71851474..72076054hg38UCSC Ensembl
Innerchr18:69518710..69743289hg19UCSC Ensembl
Innerchr18:67669690..67894269hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38224581
hg19224580
hg18224580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887275
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577608
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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