A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431864



Internal ID21393866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99499639..99500642hg38UCSC Ensembl
chr13:100151893..100152896hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381004
hg191004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750347
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431864
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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