A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438421



Internal ID21095974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73466287..73466901hg38UCSC Ensembl
chr10:75226045..75226659hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983863
Samples
Known GenesPPP3CB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438421
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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