A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609251



Internal ID20982322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155396790..155397420hg38UCSC Ensembl
chr6:155717924..155718554hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139781
Samples
Known GenesNOX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609251
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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