A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387675



Internal ID22445545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46145627..46145952hg38UCSC Ensembl
chr13:46719762..46720087hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940592
Supporting Variants
Samples
Known GenesLCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387675
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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