A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445506



Internal ID22111685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77174910..77174910hg38UCSC Ensembl
chr13:77749045..77749045hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764509
Samples
Known GenesMYCBP2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445506
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer