A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024071



Internal ID20591111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52465003..52475089hg38UCSC Ensembl
chr15:52757200..52767286hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3810087
hg1910087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509227
Supporting Variants
Samples
Known GenesMYO5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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