A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977876



Internal ID20544916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114263516..114267559hg38UCSC Ensembl
chr10:116023275..116027318hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg384044
hg194044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452921
Supporting Variants
Samples
Known GenesVWA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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