A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293119



Internal ID20502337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113314520..113314619hg38UCSC Ensembl
chr13:113968835..113968934hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735612
Supporting Variants
Samples
Known GenesLAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293119
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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