A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383832



Internal ID21041385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:117906827..117920498hg38UCSC Ensembl
chr4:118827982..118841653hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3813672
hg1913672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383832
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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