A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382196



Internal ID21039749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148506701..148529069hg38UCSC Ensembl
chr4:149427853..149450221hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3822369
hg1922369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382196
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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