A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577591



Internal ID16365000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71403379..71432372hg38UCSC Ensembl
Innerchr18:69070615..69099608hg19UCSC Ensembl
Innerchr18:67221595..67250588hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3828994
hg1928994
hg1828994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150625
SamplesNINDS_84
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577591
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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