A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984302



Internal ID20551343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88925753..88927328hg38UCSC Ensembl
chr10:90685510..90687085hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg381576
hg191576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451679
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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