A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011958



Internal ID22073589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:57130837..57140126hg38UCSC Ensembl
Outerchr18:57129427..57143056hg38UCSC Ensembl
Innerchr18:54798068..54807357hg19UCSC Ensembl
Outerchr18:54796658..54810287hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3813630
hg1913630
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155518
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011958
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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