A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371050



Internal ID21028603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72926001..72930700hg38UCSC Ensembl
chr3:72975152..72979851hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208708
Samples
Known GenesGXYLT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371050
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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