A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521188



Internal ID297484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71931092..71932793hg38UCSC Ensembl
chr15:72223433..72225134hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381702
hg191702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702408
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521188
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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