A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431199



Internal ID21393201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128960975..128963361hg38UCSC Ensembl
chr10:130759239..130761625hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382387
hg192387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749766, nssv15749290
SamplesSMI041, SMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431199
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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