A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368260



Internal ID21025813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72879359..72971806hg38UCSC Ensembl
chr3:72928510..73020957hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3892448
hg1992448
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208707
Samples
Known GenesGXYLT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368260
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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