A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865733



Internal ID22640668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76601229..76604188hg38UCSC Ensembl
chr8:77513464..77516423hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg382960
hg192960
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509906
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865733
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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