A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025279



Internal ID21934622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89790993..89791147hg38UCSC Ensembl
chr15:90334224..90334378hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609491
Samples
Known GenesANPEP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025279
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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