A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442918



Internal ID21100471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122907749..122915271hg38UCSC Ensembl
chr9:125670028..125677550hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg387523
hg197523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176512
Samples
Known GenesZBTB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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