A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979519



Internal ID20546559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110845528..110851474hg38UCSC Ensembl
chr10:112605286..112611232hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg385947
hg195947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440199
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979519
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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