A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772659



Internal ID18966917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12311990..12373591hg38UCSC Ensembl
chr8:12169499..12231100hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3861602
hg1961602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075112
Supporting Variants
SamplesKWP1
Known GenesDEFB130, FAM66A, LOC100133267
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772659
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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