A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746873



Internal ID21392976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44710803..44736802hg38UCSC Ensembl
chr15:45003001..45029000hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3826000
hg1926000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432230
Supporting Variants
SamplesSMI041
Known GenesB2M, TRIM69
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746873
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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