A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507690



Internal ID284403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62171553..62173749hg38UCSC Ensembl
chr11:61939025..61941221hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg382197
hg192197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507690
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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