A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752246



Internal ID21384808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6730323..6730871hg38UCSC Ensembl
chr8:6587844..6588392hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435544
Supporting Variants
SamplesBTQ038
Known GenesAGPAT5
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752246
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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