A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360565



Internal ID21018118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75544501..75809800hg38UCSC Ensembl
chr3:75593652..75858951hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38265300
hg19265300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4921n223
Supporting Variantsnssv18208753
Samples
Known GenesFLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360565
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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