A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382511



Internal ID21040064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120547801..120554300hg38UCSC Ensembl
chr4:121468956..121475455hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5436n223
Supporting Variantsnssv18210207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382511
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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