A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745924



Internal ID21384087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2144887..2146886hg38UCSC Ensembl
chr5:2145001..2147000hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434607
Supporting Variants
SamplesBTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745924
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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