A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922718



Internal ID22697943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10152641..10171810hg38UCSC Ensembl
chr8:10010151..10029320hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3819170
hg1919170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447785
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922718
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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