A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431269



Internal ID21393271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133291853..133292569hg38UCSC Ensembl
chr10:135105357..135106073hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15746482
SamplesNB12
Known GenesTUBGCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431269
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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