A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611497



Internal ID20984568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166481673..166482124hg38UCSC Ensembl
chr6:166895161..166895612hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140487
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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