A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877207



Internal ID22652170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:90073000..90081070hg38UCSC Ensembl
chr16:90139408..90147478hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg388071
hg198071
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474797, nssv17474798
Samples
Known GenesPRDM7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877207
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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