A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501618



Internal ID278512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10301276..10303403hg38UCSC Ensembl
chr11:10322823..10324950hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382128
hg192128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501618
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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