A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926771



Internal ID22701998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5729077..5729428hg38UCSC Ensembl
chr10:5771040..5771391hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359227
Samples
Known GenesFAM208B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926771
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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