A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371388



Internal ID21028941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30780397..30797000hg38UCSC Ensembl
chr3:30821889..30838492hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3816604
hg1916604
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210500
Samples
Known GenesGADL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371388
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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