A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458953



Internal ID236972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24418236..24418457hg38UCSC Ensembl
chr6:24418464..24418685hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980164
Samples
Known GenesMRS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458953
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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