A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385225



Internal ID22443095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88901183..88901244hg38UCSC Ensembl
chr15:89444414..89444475hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940726
Supporting Variants
Samples
Known GenesMFGE8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385225
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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