A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471772



Internal ID22529664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71321891..71344210hg38UCSC Ensembl
chr15:71614230..71636549hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3822320
hg1922320
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853813
Supporting Variants
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471772
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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