A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409112



Internal ID21066665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73511594..73512531hg38UCSC Ensembl
chr6:74221317..74222254hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409112
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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