A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981652



Internal ID20548692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43451201..43470600hg38UCSC Ensembl
chr10:43946649..43966048hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3819400
hg1919400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447092
Supporting Variants
Samples
Known GenesZNF487
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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