A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850878



Internal ID22625813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34977229..34985108hg38UCSC Ensembl
chr8:34834747..34842626hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg387880
hg197880
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850878
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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