A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386040



Internal ID22443910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95975960..95976120hg38UCSC Ensembl
chr13:96628214..96628374hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928355
Supporting Variants
Samples
Known GenesUGGT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386040
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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