A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389645



Internal ID21047198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51936918..51949330hg38UCSC Ensembl
chr4:52803084..52815496hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3812413
hg1912413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211893
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389645
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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