A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772511



Internal ID19313068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11025689..11027290hg38UCSC Ensembl
chr8:10883199..10884800hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077515
Supporting Variants
SamplesKWP1
Known GenesXKR6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772511
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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