A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376679



Internal ID22602348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35574143..35578834hg38UCSC Ensembl
chr13:36148280..36152971hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg384692
hg194692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939286
Supporting Variants
Samples
Known GenesMIR548F5, NBEA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376679
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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