A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15768491



Internal ID22102962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179871726..179871867hg38UCSC Ensembl
chr5:179298726..179298867hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4443538
Supporting Variants
Samples
Known GenesTBC1D9B
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15768491
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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