A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1525n106



Internal ID20160882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82412000..82412110hg38UCSC Ensembl
chr17:80369876..80369986hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1143688, nsv1134685
SamplesKWS1, KWS2
Known GenesOGFOD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1525n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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