A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864023



Internal ID22638958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66937974..66939183hg38UCSC Ensembl
chr8:67850209..67851418hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg381210
hg191210
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509709, nssv17509710
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864023
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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