A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765764



Internal ID18958149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26291483..26292484hg38UCSC Ensembl
chr8:26148999..26150000hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076075
Supporting Variants
SamplesKWP1
Known GenesPPP2R2A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765764
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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