A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386678



Internal ID21044231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37877884..37879976hg38UCSC Ensembl
chr4:37879505..37881597hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382093
hg192093
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386678
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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