A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053618



Internal ID103590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118541263..118542970hg38UCSC Ensembl
chr11:118411978..118413685hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381708
hg191708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494546
Supporting Variants
Samples
Known GenesTMEM25
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053618
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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