A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1170n106



Internal ID22794998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22472167..22482396hg38UCSC Ensembl
chr15:23390700..23402300hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3810230
hg1911601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1124702, nsv1132407
SamplesKWS2, KWS1
Known GenesHERC2P7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1170n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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