A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618520



Internal ID20991591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155428140..155430495hg38UCSC Ensembl
chr6:155749274..155751629hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382356
hg192356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139783
Samples
Known GenesNOX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618520
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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