A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199658



Internal ID21338454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139872728..139872928hg38UCSC Ensembl
chr8:140884972..140885172hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3946514
Supporting Variants
SamplesHG002
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199658
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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