A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359227



Internal ID22584896
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 StatusS
Merged Variantsnsv5926771
Supporting Variants
Samples
Known GenesFAM208B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359227
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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