A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190129



Internal ID20757169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58080427..58132834hg38UCSC Ensembl
chr10:59840187..59892595hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3852408
hg1952409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440528
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190129
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00099


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