A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183692



Internal ID20750732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76662774..76861389hg38UCSC Ensembl
chr10:78422532..78621147hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38198616
hg19198616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440309
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183692
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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