A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446168



Internal ID22112347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196334782..196334993hg38UCSC Ensembl
chr3:196061653..196061864hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761507
Samples
Known GenesTM4SF19, TM4SF19-TCTEX1D2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446168
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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