A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619847



Internal ID20992918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127484887..127485401hg38UCSC Ensembl
chr6:127806032..127806546hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137681
Samples
Known GenesSOGA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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