A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15750939



Internal ID21386802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54012982..54013680hg38UCSC Ensembl
chr8:54925542..54926240hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435521
Supporting Variants
SamplesMDQ025
Known GenesTCEA1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15750939
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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