A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044290



Internal ID97264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36266861..36267686hg38UCSC Ensembl
chr11:36288411..36289236hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507476
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044290
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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