A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046303



Internal ID20613343
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 StatusS
Merged Variantsnsv6529278
Supporting Variants
Samples
Known GenesCOX6B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046303
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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