A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3851n106



Internal ID22797679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78771162..78771263hg38UCSC Ensembl
chr8:79683397..79683498hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1123737, nsv1131894
SamplesKWS1
Known GenesIL7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3851n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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