A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386235



Internal ID21043788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41597311..41610364hg38UCSC Ensembl
chr5:41597413..41610466hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3813054
hg1913054
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386235
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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