A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614716



Internal ID20987787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127454564..127454997hg38UCSC Ensembl
chr6:127775709..127776142hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137678
Samples
Known GenesKIAA0408, SOGA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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