A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182122



Internal ID20749162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62229176..62287650hg38UCSC Ensembl
chr10:63988935..64047409hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3858475
hg1958475
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440153
Supporting Variants
Samples
Known GenesRTKN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182122
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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