A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702024



Internal ID125690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74820087..74820190hg38UCSC Ensembl
chr15:75112428..75112531hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517531
Supporting Variants
Samples
Known GenesLMAN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702024
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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