A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922948



Internal ID22698173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:131442932..131556123hg38UCSC Ensembl
chr8:132455179..132568370hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38113192
hg19113192
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922948
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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