A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446399



Internal ID22112578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61071213..61071213hg38UCSC Ensembl
chr15:61363412..61363412hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761392
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446399
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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