A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577598



Internal ID16365007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71725624..71927163hg38UCSC Ensembl
Innerchr18:69392860..69594399hg19UCSC Ensembl
Innerchr18:67543840..67745379hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38201540
hg19201540
hg18201540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150627
Samples1782681164_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577598
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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