A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041333



Internal ID95262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10326743..10327574hg38UCSC Ensembl
chr11:10348290..10349121hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500327
Supporting Variants
Samples
Known GenesCAND1.11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041333
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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