A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15750432



Internal ID21393115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11146038..11187037hg38UCSC Ensembl
chr10:11188001..11229000hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3841000
hg1941000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431154
Supporting Variants
SamplesSMI041
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15750432
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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