A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506792



Internal ID283527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27783797..27784354hg38UCSC Ensembl
chr12:27936730..27937287hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17055104
Samples
Known GenesKLHL42
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506792
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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