A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862979



Internal ID22637914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74874825..74881516hg38UCSC Ensembl
chr8:75787060..75793751hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg386692
hg196692
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862979
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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