A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384665



Internal ID21042218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52443194..52500652hg38UCSC Ensembl
chr4:53309360..53366818hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3857459
hg1957459
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211905
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384665
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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