A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853019



Internal ID22627954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71210833..71221739hg38UCSC Ensembl
chr15:71503172..71514078hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3810907
hg1910907
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473578
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853019
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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