A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190741



Internal ID20757781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97328367..97339810hg38UCSC Ensembl
chr10:99088124..99099567hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3811444
hg1911444
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436487
Supporting Variants
Samples
Known GenesFRAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190741
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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