A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766114



Internal ID19305572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27240891..27266592hg38UCSC Ensembl
chr19:27731799..27757500hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg3825702
hg1925702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078441
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766114
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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