A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439182



Internal ID22105359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23704136..23704136hg38UCSC Ensembl
chr9:23704134..23704134hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757978
Samples
Known GenesELAVL2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439182
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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