A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186139



Internal ID20753179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9341531..9350194hg38UCSC Ensembl
chr11:9363078..9371741hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388664
hg198664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439395
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186139
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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