A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435219



Internal ID21092772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137751974..137752419hg38UCSC Ensembl
chr8:138764217..138764662hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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