A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978590



Internal ID20545630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13302808..13305610hg38UCSC Ensembl
chr10:13344808..13347610hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382803
hg192803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444681
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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