A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408660



Internal ID21066213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75685777..75687965hg38UCSC Ensembl
chr6:76395493..76397681hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382189
hg192189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145216
Samples
Known GenesSENP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408660
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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