A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747334



Internal ID21392531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:21476892..21572891hg38UCSC Ensembl
chr5:21477001..21573000hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3896000
hg1996000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434616
Supporting Variants
SamplesSMI034
Known GenesGUSBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747334
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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