A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981653



Internal ID20548693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43463172..43468675hg38UCSC Ensembl
chr10:43958620..43964123hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg385504
hg195504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444897
Supporting Variants
Samples
Known GenesZNF487
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981653
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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