A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455172



Internal ID21112725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104229401..104234900hg38UCSC Ensembl
chr10:105989159..105994658hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181675
Samples
Known GenesWDR96
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455172
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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