A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431152



Internal ID21088705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17193113..17193877hg38UCSC Ensembl
chr8:17050622..17051386hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166297
Samples
Known GenesZDHHC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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