A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501636



Internal ID278529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35603625..35603782hg38UCSC Ensembl
chr11:35625173..35625330hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501636
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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