A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444284



Internal ID21101837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83886723..83942608hg38UCSC Ensembl
chr10:85646479..85702364hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3855886
hg1955886
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196067
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444284
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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