A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535849



Internal ID311432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29148708..29149414hg38UCSC Ensembl
chr22:29544696..29545402hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728345
Samples
Known GenesKREMEN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535849
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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