A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529278



Internal ID20902639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35653508..35653804hg38UCSC Ensembl
chr19:36144410..36144706hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046303
Samples
Known GenesCOX6B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529278
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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