A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431141



Internal ID21393143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99312231..99319825hg38UCSC Ensembl
chr10:101071988..101079582hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg387595
hg197595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752442
SamplesNB07
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431141
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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