A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755907



Internal ID20531767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91134507..91134507hg38UCSC Ensembl
chr13:91786761..91786761hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283520
Samples
Known GenesLINC00379
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755907
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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