A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612955



Internal ID20986026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167827701..167832800hg38UCSC Ensembl
chr6:168228381..168233480hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216032
Samples
Known GenesMLLT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612955
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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