A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381784



Internal ID21039337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109032502..109484409hg38UCSC Ensembl
chr4:109953658..110405565hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38451908
hg19451908
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209515
Samples
Known GenesCOL25A1, SEC24B, SEC24B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381784
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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