A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977394



Internal ID20544435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:108335540..108341390hg38UCSC Ensembl
chr10:110095298..110101148hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg385851
hg195851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438930
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977394
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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