A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382354



Internal ID22440224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69381587..69385672hg38UCSC Ensembl
chr15:69673926..69678011hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384086
hg194086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929873
Supporting Variants
Samples
Known GenesPAQR5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382354
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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