A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983864



Internal ID20550904
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 StatusS
Merged Variantsnsv6451107
Supporting Variants
Samples
Known GenesPPP3CB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983864
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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