A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382262



Internal ID21039815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139906360..139913631hg38UCSC Ensembl
chr4:140827514..140834785hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg387272
hg197272
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213047
Samples
Known GenesMAML3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382262
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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