A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509973



Internal ID286606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74847070..74847159hg38UCSC Ensembl
chr11:74558115..74558204hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047177
Samples
Known GenesXRRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509973
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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