A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445186



Internal ID22111366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36688478..36688478hg38UCSC Ensembl
chr1:37154079..37154079hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765404
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445186
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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