A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980333



Internal ID20547373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44356186..44360712hg38UCSC Ensembl
chr10:44851634..44856160hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg384527
hg194527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453402
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980333
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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