A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495768



Internal ID272866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67452074..67453545hg38UCSC Ensembl
chr11:67219545..67221016hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381472
hg191472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046248
Samples
Known GenesGPR152
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495768
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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