A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447392



Internal ID22113569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101241788..101244068hg38UCSC Ensembl
chr13:101894139..101896419hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382281
hg192281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761657
Samples
Known GenesNALCN
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447392
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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