A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372667



Internal ID21030220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14995501..15001700hg38UCSC Ensembl
chr4:14997125..15003324hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212067
Samples
Known GenesCPEB2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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