A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765204



Internal ID20541064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46719015..46719015hg38UCSC Ensembl
chr13:47293150..47293150hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290735
Samples
Known GenesLRCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765204
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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