A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4111n106



Internal ID20163468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103014737..103014806hg38UCSC Ensembl
chr9:105777019..105777088hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1143379, nsv1112483
SamplesKWS1, KWS2
Known GenesCYLC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4111n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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