A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507709



Internal ID284422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35560279..35566077hg38UCSC Ensembl
chr11:35581827..35587625hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385799
hg195799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507709
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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