A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983861



Internal ID20550901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73417831..73418164hg38UCSC Ensembl
chr10:75177589..75177922hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443986
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.04984


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