A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451107



Internal ID21108660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73480590..73486419hg38UCSC Ensembl
chr10:75240348..75246177hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg385830
hg195830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983864
Samples
Known GenesPPP3CB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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