A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445249



Internal ID22111429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39044557..39044557hg38UCSC Ensembl
chr1:39510229..39510229hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758744
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445249
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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