A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863272



Internal ID22638207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38476586..38478685hg38UCSC Ensembl
chr8:38334104..38336203hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863272
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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