A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382310



Internal ID21039863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:66499373..66533043hg38UCSC Ensembl
chr4:67365091..67398761hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3833671
hg1933671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382310
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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