A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15759297



Internal ID22093751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109488948..109488948hg38UCSC Ensembl
chr13:110141295..110141295hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4443898
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15759297
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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