A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15759260



Internal ID22093736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:47940860..47940860hg38UCSC Ensembl
chr12:48334643..48334643hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4437563
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15759260
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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