A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440770



Internal ID21098323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43381890..43389191hg38UCSC Ensembl
chr10:43877338..43884639hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg387302
hg197302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185420
Samples
Known GenesHNRNPF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440770
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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