A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765297



Internal ID19310831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29295982..29305883hg38UCSC Ensembl
chr8:29153499..29163400hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg389902
hg199902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077523
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765297
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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