A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688361



Internal ID112027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35181055..35181927hg38UCSC Ensembl
chr11:35202602..35203474hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513873
Supporting Variants
Samples
Known GenesCD44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688361
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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