A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445184



Internal ID22111364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35260187..35260187hg38UCSC Ensembl
chr1:35725788..35725788hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765402
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445184
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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