A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979329



Internal ID20546369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2568057..2571672hg38UCSC Ensembl
chr10:2610249..2613864hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383616
hg193616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446160
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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