A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749766



Internal ID21391700
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 StatusS
Merged Variantsnsv4431199
Supporting Variants
SamplesSMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749766
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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