A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429129



Internal ID21086682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17186921..17187713hg38UCSC Ensembl
chr8:17044430..17045222hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38793
hg19793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166296
Samples
Known GenesZDHHC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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