A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193103



Internal ID20760143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62725798..62735376hg38UCSC Ensembl
chr10:64485558..64495136hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg389579
hg199579
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193103
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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