A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475579



Internal ID22533475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99568294..99569643hg38UCSC Ensembl
chr15:100108499..100109848hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872964
Supporting Variants
Samples
Known GenesMEF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475579
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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