A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388037



Internal ID22445907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99567815..99567890hg38UCSC Ensembl
chr15:100108020..100108095hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942174
Supporting Variants
Samples
Known GenesMEF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388037
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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