A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441437



Internal ID22107617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10723897..10723897hg38UCSC Ensembl
chr4:10725521..10725521hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757218
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441437
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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