A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370472



Internal ID22596141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113750638..113750820hg38UCSC Ensembl
chr13:114453611..114453793hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936785
Supporting Variants
Samples
Known GenesLINC00552
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370472
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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