A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397283



Internal ID21054836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14959866..14972141hg38UCSC Ensembl
chr6:14960097..14972372hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3812276
hg1912276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217088
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397283
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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