A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362925



Internal ID21020478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26319001..26322500hg38UCSC Ensembl
chr4:26320623..26324122hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211829
Samples
Known GenesRBPJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362925
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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