A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377233



Internal ID21034786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43371883..43684119hg38UCSC Ensembl
chr4:43373900..43686136hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38312237
hg19312237
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377233
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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