A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431155



Internal ID21393157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11283038..11285037hg38UCSC Ensembl
chr10:11325001..11327000hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750321, nssv15747089, nssv15748895, nssv15747613
SamplesNB12, NB10, BTQ016, NB07
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431155
Frequency
Sample Size15
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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