A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3026n106



Internal ID22796854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2512272..2512423hg38UCSC Ensembl
chr5:2512386..2512537hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121318, nsv1111663
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3026n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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