A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208722



Internal ID20775762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75098572..75711134hg38UCSC Ensembl
chr3:75147723..75760285hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38612563
hg19612563
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373879
Supporting Variants
Samples
Known GenesFAM86DP, FLJ20518, FRG2C, LINC00960, MIR1324, MIR4444-1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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