A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431152



Internal ID21393154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106190998..106191945hg38UCSC Ensembl
chr10:107950756..107951703hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38948
hg19948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv94n172
Supporting Variantsnssv15749404
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431152
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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