A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450531



Internal ID21108084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100052419..100057598hg38UCSC Ensembl
chr10:101812176..101817355hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg385180
hg195180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977165
Samples
Known GenesCPN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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