A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766148



Internal ID22100619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29835083..29835137hg38UCSC Ensembl
chr13:30409220..30409274hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4446381
Supporting Variants
Samples
Known GenesUBL3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766148
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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