A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920774



Internal ID22695997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100573155..100573230hg38UCSC Ensembl
chr8:101585383..101585458hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446561
Samples
Known GenesSNX31
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920774
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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