A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1449n106



Internal ID22795277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:26936074..27010574hg38UCSC Ensembl
chr17:25263100..25337600hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3874501
hg1974501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1115518, nsv1128761
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1449n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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