A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435298



Internal ID21092851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:4214009..4329261hg38UCSC Ensembl
chr8:4071531..4186783hg19UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38115253
hg19115253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166944
Samples
Known GenesCSMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435298
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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