A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15763649



Internal ID22098131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106775337..106775389hg38UCSC Ensembl
chr13:107427685..107427737hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4447779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15763649
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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