A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025491



Internal ID21934834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113313919..113314016hg38UCSC Ensembl
chr13:113968234..113968331hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614522
Samples
Known GenesLAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025491
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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