A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979677



Internal ID20546717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22612401..22614500hg38UCSC Ensembl
chr10:22901330..22903429hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441863
Supporting Variants
Samples
Known GenesPIP4K2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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