A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761362



Internal ID22095856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4243729..4243729hg38UCSC Ensembl
chr12:4352895..4352895hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4449069
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761362
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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