A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609433



Internal ID20982504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139278781..139280030hg38UCSC Ensembl
chr6:139599918..139601167hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381250
hg191250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138424
Samples
Known GenesTXLNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609433
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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