A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438085



Internal ID22495955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140094836..140095987hg38UCSC Ensembl
chr8:141104935..141106086hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381152
hg191152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917309
Supporting Variants
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438085
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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