A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178088



Internal ID20745128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77415201..77419600hg38UCSC Ensembl
chr15:77707543..77711942hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499877
Supporting Variants
Samples
Known GenesPEAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178088
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00059


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