A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190514



Internal ID20757554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50714939..50731538hg38UCSC Ensembl
chr10:52474699..52491298hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3816600
hg1916600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437982
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190514
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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