A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038910



Internal ID21948253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96966735..96981062hg38UCSC Ensembl
chr15:97509965..97524292hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3814328
hg1914328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038910
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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