A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855024



Internal ID22629959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45419173..45424003hg38UCSC Ensembl
chr15:45711371..45716201hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg384831
hg194831
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471660
Samples
Known GenesSPATA5L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855024
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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