A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448629



Internal ID22114806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66522240..66522240hg38UCSC Ensembl
chr5:65818068..65818068hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767773
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448629
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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