A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749404



Internal ID21387686
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 StatusS
Merged Variantsnsv4431152
Supporting Variants
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749404
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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