A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910156



Internal ID22685366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132752690..132753330hg38UCSC Ensembl
chr8:133764936..133765576hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436374
Samples
Known GenesTMEM71
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910156
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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