A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181706



Internal ID20748746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64302963..64311595hg38UCSC Ensembl
chr11:64070435..64079067hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg388633
hg198633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458490
Supporting Variants
Samples
Known GenesESRRA, TEX40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181706
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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