A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764850



Internal ID19313725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29320682..29329383hg38UCSC Ensembl
chr8:29178199..29186900hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg388702
hg198702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076646
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764850
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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