A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378970



Internal ID21036523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120548801..120554400hg38UCSC Ensembl
chr4:121469956..121475555hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5436n223
Supporting Variantsnssv18210208
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378970
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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