A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433562



Internal ID21091115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76833817..76834412hg38UCSC Ensembl
chr8:77746053..77746648hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171388
Samples
Known GenesZFHX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433562
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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