A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3872n106



Internal ID22797700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105533572..105534372hg38UCSC Ensembl
chr8:106545800..106546600hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1119184, nsv1137619
SamplesKWS2, KWS1
Known GenesZFPM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3872n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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