A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507916



Internal ID284621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108376000..108386364hg38UCSC Ensembl
chr11:108246727..108257091hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3810365
hg1910365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049124
Samples
Known GenesC11orf65
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507916
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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