A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431151



Internal ID21393153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106190927..106191954hg38UCSC Ensembl
chr10:107950685..107951712hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381028
hg191028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv94n172
Supporting Variantsnssv15749877
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431151
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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