A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1061n106



Internal ID22794889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30474394..30479094hg38UCSC Ensembl
chr14:30943600..30948300hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg384701
hg194701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1132383, nsv1115459
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1061n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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