A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768415



Internal ID19312142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22598886..22599787hg38UCSC Ensembl
chr8:22456399..22457300hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077027
Supporting Variants
SamplesKWP1
Known GenesC8orf58
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768415
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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