A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925639



Internal ID22700866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140099111..140099205hg38UCSC Ensembl
chr8:141109210..141109304hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431827
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925639
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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