A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3860n106



Internal ID20163217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91140628..91140953hg38UCSC Ensembl
chr8:92152856..92153181hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135714, nsv1111740
SamplesKWS1, KWS2
Known GenesLRRC69
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3860n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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