A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493938



Internal ID271100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37940512..37940820hg38UCSC Ensembl
chr11:37962062..37962370hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493938
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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