A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497705



Internal ID274730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33929270..33929371hg38UCSC Ensembl
chr11:33950817..33950918hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497705
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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