A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441781



Internal ID22107962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118940825..118940825hg38UCSC Ensembl
chr6:119261990..119261990hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762026
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441781
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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