A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381994



Internal ID21039547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42079882..42090875hg38UCSC Ensembl
chr4:42081899..42092892hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3810994
hg1910994
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213640
Samples
Known GenesSLC30A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381994
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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