A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190125



Internal ID20757165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69837702..69840157hg38UCSC Ensembl
chr10:71597458..71599913hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382456
hg192456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444720
Supporting Variants
Samples
Known GenesCOL13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190125
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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