A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494972



Internal ID272099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132319287..132320281hg38UCSC Ensembl
chr11:132189181..132190175hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053557
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494972
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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