A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884913



Internal ID22659897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89161646..89163345hg38UCSC Ensembl
chr15:89704877..89706576hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472382
Samples
Known GenesABHD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884913
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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