A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439490



Internal ID22105668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15415619..15415619hg38UCSC Ensembl
chr6:15415850..15415850hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757341
Samples
Known GenesJARID2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439490
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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