A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4019984



Internal ID22081615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8466095..8591178hg38UCSC Ensembl
Outerchr8:8462519..8592908hg38UCSC Ensembl
Innerchr8:8323605..8448688hg19UCSC Ensembl
Outerchr8:8320029..8450418hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38130390
hg19130390
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156834
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4019984
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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