A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378263



Internal ID21035816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102684546..102725637hg38UCSC Ensembl
chr4:103605703..103646794hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3841092
hg1941092
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209445
Samples
Known GenesMANBA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378263
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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