A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208751



Internal ID20775791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75544001..75812900hg38UCSC Ensembl
chr3:75593152..75862051hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38268900
hg19268900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361648
Supporting Variants
Samples
Known GenesFLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208751
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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