A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15760463



Internal ID22094952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193511660..193511660hg38UCSC Ensembl
chr3:193229449..193229449hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4440549
Supporting Variants
Samples
Known GenesATP13A4
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15760463
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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