A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427600



Internal ID21085153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39962515..39962710hg38UCSC Ensembl
chr8:39820034..39820229hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167983
Samples
Known GenesIDO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427600
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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