A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378851



Internal ID22436721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77203964..77255515hg38UCSC Ensembl
chr15:77496306..77547857hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3851552
hg1951552
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945672
Supporting Variants
Samples
Known GenesLINC00597, PEAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378851
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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