A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15760397



Internal ID22094879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109569155..109569291hg38UCSC Ensembl
chr13:110221502..110221638hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4447547
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15760397
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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