A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440763



Internal ID22106941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69816453..69816453hg38UCSC Ensembl
chr6:70526345..70526345hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766253
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440763
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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