A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849888



Internal ID22624823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75424562..75432743hg38UCSC Ensembl
chr10:77184320..77192501hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg388182
hg198182
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455244, nssv17456282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849888
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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