A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377763



Internal ID22435633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52335923..52336007hg38UCSC Ensembl
chr15:52628120..52628204hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937113
Supporting Variants
Samples
Known GenesMYO5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377763
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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