A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855318



Internal ID22630253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71384023..71389601hg38UCSC Ensembl
chr15:71676362..71681940hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385579
hg195579
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473590
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855318
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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