A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913701



Internal ID22688917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85068815..85068865hg38UCSC Ensembl
chr8:85981050..85981100hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444666
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913701
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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