A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442241



Internal ID21099794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7944056..7951680hg38UCSC Ensembl
chr10:7986019..7993643hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg387625
hg197625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194527
Samples
Known GenesTAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442241
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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