A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753011



Internal ID21387904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32195613..32200323hg38UCSC Ensembl
chr5:32195719..32200429hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg384711
hg194711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434632
Supporting Variants
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753011
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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