A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897246



Internal ID22672346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155409156..155409230hg38UCSC Ensembl
chr6:155730290..155730364hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424580
Samples
Known GenesNOX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897246
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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