A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923777



Internal ID22699004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125472569..125472909hg38UCSC Ensembl
chr8:126484811..126485151hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923777
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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