A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745832



Internal ID21389470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106190927..106191837hg38UCSC Ensembl
chr10:107950685..107951595hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431150
Supporting Variants
SamplesNB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745832
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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