A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208737



Internal ID20775777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75372001..75811700hg38UCSC Ensembl
chr3:75421152..75860851hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38439700
hg19439700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369575
Supporting Variants
Samples
Known GenesFAM86DP, FLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208737
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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