A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979473



Internal ID20546513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109671001..109674500hg38UCSC Ensembl
chr10:111430759..111434258hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443567
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979473
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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