A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520206



Internal ID296540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72171325..72178551hg38UCSC Ensembl
chr15:72463666..72470892hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg387227
hg197227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702424
Samples
Known GenesGRAMD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520206
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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