A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967929



Internal ID22742864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113260203..113260203hg38UCSC Ensembl
chr13:113914517..113914517hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378883
Samples
Known GenesCUL4A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967929
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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