A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500678



Internal ID277606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95277009..95280597hg38UCSC Ensembl
chr11:95010173..95013761hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383589
hg193589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050055
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500678
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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