A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404206



Internal ID21061759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85446759..85452415hg38UCSC Ensembl
chr6:86156477..86162133hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg385657
hg195657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146050
Samples
Known GenesNT5E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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