A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388572



Internal ID22446442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89200373..89200373hg38UCSC Ensembl
chr15:89743604..89743604hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976684
Supporting Variants
Samples
Known GenesABHD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388572
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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