A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748012



Internal ID21388647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196897130..196899129hg38UCSC Ensembl
chr3:196624001..196626000hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434028
Supporting Variants
SamplesNB08
Known GenesSENP5
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748012
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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