A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946729



Internal ID22722225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89161675..89163435hg38UCSC Ensembl
chr15:89704906..89706666hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381761
hg191761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371794
Samples
Known GenesABHD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946729
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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