A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15750489



Internal ID21393122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22604072..22684071hg38UCSC Ensembl
chr10:22893001..22973000hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3880000
hg1980000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431289
Supporting Variants
SamplesSMI041
Known GenesPIP4K2A
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15750489
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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