A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751425



Internal ID21385073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45026803..45031802hg38UCSC Ensembl
chr15:45319001..45324000hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432231
Supporting Variants
SamplesBTQ038
Known GenesSORD
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751425
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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