A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026593



Internal ID21935936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88538641..88545721hg38UCSC Ensembl
chr15:89081872..89088952hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg387081
hg197081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606307
Samples
Known GenesDET1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026593
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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