A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433800



Internal ID21091353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19479401..19485200hg38UCSC Ensembl
chr8:19336912..19342711hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165355
Samples
Known GenesCSGALNACT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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