A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381826



Internal ID22439696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35151093..35151308hg38UCSC Ensembl
chr17:33478112..33478327hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943555
Supporting Variants
Samples
Known GenesUNC45B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381826
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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