A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1335n106



Internal ID22795163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29621479..29631079hg38UCSC Ensembl
chr16:29632800..29642400hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg389601
hg199601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1139653, nsv1110273
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1335n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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