A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432000



Internal ID21394002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40695752..40697287hg38UCSC Ensembl
chr13:41269888..41271423hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381536
hg191536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751310
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432000
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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