A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3934n106



Internal ID20163291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144465417..144466117hg38UCSC Ensembl
chr8:145690800..145691500hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1144243, nsv1112975
SamplesKWS1, KWS2
Known GenesCYHR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3934n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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