A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194751



Internal ID20761791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86597936..86721585hg38UCSC Ensembl
chr10:88357693..88481342hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38123650
hg19123650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445257
Supporting Variants
Samples
Known GenesLDB3, OPN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194751
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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