A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421597



Internal ID21079150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96611200..96611593hg38UCSC Ensembl
chr8:97623428..97623821hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173795
Samples
Known GenesSDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421597
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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