A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5504206



Internal ID281014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131753615..131777607hg38UCSC Ensembl
chr11:131623509..131647501hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3823993
hg1923993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053828
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5504206
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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