A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3803n106



Internal ID20163160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31713725..31714091hg38UCSC Ensembl
chr8:31571241..31571607hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1130151, nsv1117139, nsv1121401
SamplesKWS1, KWS2
Known GenesNRG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3803n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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