A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354522



Internal ID22580191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101469617..101481590hg38UCSC Ensembl
chr13:102121968..102133941hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3811974
hg1911974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945877
Supporting Variants
Samples
Known GenesITGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354522
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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