A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2096n106



Internal ID20161453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174225897..174226218hg38UCSC Ensembl
chr2:175090625..175090946hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1126722, nsv1136180
SamplesKWS1
Known GenesOLA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2096n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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