A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956972



Internal ID22732125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33986965..33986965hg38UCSC Ensembl
chr8:33844483..33844483hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441687
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956972
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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