A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026773



Internal ID21936116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82095923..82095989hg38UCSC Ensembl
chr15:82388264..82388330hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026773
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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