A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2062n106



Internal ID20161419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:152348808..152349142hg38UCSC Ensembl
chr2:153205322..153205656hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120763, nsv1121218
SamplesKWS2
Known GenesFMNL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2062n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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