A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865803



Internal ID22640738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71351684..71379447hg38UCSC Ensembl
chr15:71644023..71671786hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3827764
hg1927764
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473586
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865803
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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