A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984564



Internal ID20551605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83784801..83791900hg38UCSC Ensembl
chr10:85544557..85551656hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443482
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00107


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