A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7365n223



Internal ID22810333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61599401..61603200hg38UCSC Ensembl
chr8:62511960..62515759hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6419628, nsv6427250
Samples
Known GenesASPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7365n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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