A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609547



Internal ID20982618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102332842..102339553hg38UCSC Ensembl
chr6:102780717..102787428hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg386712
hg196712
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216497
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609547
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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