A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441720



Internal ID22107901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39408925..39408925hg38UCSC Ensembl
chr4:39410545..39410545hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763554
Samples
Known GenesKLB, MIR1273H
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441720
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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