A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3797n106



Internal ID19021906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25208784..25213204hg38UCSC Ensembl
chr8:25066300..25070720hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg384421
hg194421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135701, nsv1135385, nsv1120930, nsv1129413, nsv1117132
SamplesKWS1, KWS2
Known GenesDOCK5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3797n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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