A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924901



Internal ID22700128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:136656644..137924603hg38UCSC Ensembl
chr8:137668887..138936846hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg381267960
hg191267960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924901
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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