A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423984



Internal ID21081537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22799053..22804373hg38UCSC Ensembl
chr8:22656566..22661886hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg385321
hg195321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167106
Samples
Known GenesPEBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423984
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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