A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445726



Internal ID22111903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47179098..47179098hg38UCSC Ensembl
chr1:47644770..47644770hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767837
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445726
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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