A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761242



Internal ID22095732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109357617..109357715hg38UCSC Ensembl
chr12:109795422..109795520hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445623
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761242
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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