A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909831



Internal ID22685041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52122868..52122928hg38UCSC Ensembl
chr8:53035428..53035488hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448269
Samples
Known GenesST18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909831
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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