A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979130



Internal ID20546170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20840501..20842600hg38UCSC Ensembl
chr10:21129430..21131529hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447325
Supporting Variants
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979130
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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