A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916632



Internal ID22691851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13102342..13102448hg38UCSC Ensembl
chr8:12959851..12959957hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430703
Samples
Known GenesDLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916632
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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