A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445772



Internal ID22111949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84768797..84768797hg38UCSC Ensembl
chr1:85234480..85234480hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763720
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445772
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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