A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446428



Internal ID22112607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33618454..33619184hg38UCSC Ensembl
chr13:34192591..34193321hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762877
Samples
Known GenesSTARD13
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446428
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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