A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619146



Internal ID20992217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102967375..102986052hg38UCSC Ensembl
chr6:103415250..103433927hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3818678
hg1918678
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619146
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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