A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191541



Internal ID20758581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134308987..134754393hg38UCSC Ensembl
chr11:134178881..134624287hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38445407
hg19445407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473177
Supporting Variants
Samples
Known GenesB3GAT1, GLB1L2, GLB1L3, LOC283177
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191541
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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