A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438798



Internal ID21096351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:55544164..55708047hg38UCSC Ensembl
chr10:57303924..57467807hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38163884
hg19163884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179196
Samples
Known GenesMTRNR2L5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438798
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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