A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977132



Internal ID20544172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100394941..100397878hg38UCSC Ensembl
chr10:102154698..102157635hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg382938
hg192938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436041
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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