A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866134



Internal ID22641069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36203631..36215692hg38UCSC Ensembl
chr8:36061149..36073210hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3812062
hg1912062
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866134
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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