A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179772



Internal ID20746812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43316924..43360898hg38UCSC Ensembl
chr10:43812372..43856346hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3843975
hg1943975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449614
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179772
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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