A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450798



Internal ID21108351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96314642..96320342hg38UCSC Ensembl
chr10:98074399..98080099hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg385701
hg195701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985920
Samples
Known GenesDNTT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450798
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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