A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453193



Internal ID21110746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:81695981..81700412hg38UCSC Ensembl
chr10:83455737..83460168hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384432
hg194432
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453193
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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