A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929059



Internal ID22704307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71129340..71421536hg38UCSC Ensembl
chr15:71421679..71713875hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38292197
hg19292197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385167
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929059
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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