A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471660



Internal ID22529552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45419173..45424003hg38UCSC Ensembl
chr15:45711371..45716201hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg384831
hg194831
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855024
Supporting Variants
Samples
Known GenesSPATA5L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471660
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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