A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441442



Internal ID21098995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14591839..14637738hg38UCSC Ensembl
chr10:14633838..14679737hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3845900
hg1945900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188593
Samples
Known GenesFAM107B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441442
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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