A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194388



Internal ID20761428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124852654..124857265hg38UCSC Ensembl
chr10:126541223..126545834hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384612
hg194612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194388
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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