A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439041



Internal ID21096594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102082429..102086982hg38UCSC Ensembl
chr10:103842186..103846739hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg384554
hg194554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439041
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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