A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427823



Internal ID21085376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35363206..35363691hg38UCSC Ensembl
chr8:35220724..35221209hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167399
Samples
Known GenesUNC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427823
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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