A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611552



Internal ID21803599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113314567..113314567hg38UCSC Ensembl
chr13:113968882..113968882hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094809
Supporting Variants
Samples
Known GenesLAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611552
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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