A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443824



Internal ID22110005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113263145..113263145hg38UCSC Ensembl
chr13:113917459..113917459hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381178
hg191178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764775
Samples
Known GenesCUL4A
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443824
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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