A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979337



Internal ID20546377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25820793..25822961hg38UCSC Ensembl
chr10:26109722..26111890hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg382169
hg192169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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