A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577484



Internal ID16364893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69280112..69316645hg38UCSC Ensembl
Innerchr18:66947348..66983881hg19UCSC Ensembl
Innerchr18:65098328..65134861hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3836534
hg1936534
hg1836534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150614
SamplesHGDP01297
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577484
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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