A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377000



Internal ID21034553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:117945694..117961043hg38UCSC Ensembl
chr4:118866849..118882198hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3815350
hg1915350
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211347
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377000
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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