A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980335



Internal ID20547375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44363998..44365256hg38UCSC Ensembl
chr10:44859446..44860704hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381259
hg191259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980335
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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