A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3021n106



Internal ID19021130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1291494..1291657hg38UCSC Ensembl
chr5:1291609..1291772hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1131265, nsv1138265
SamplesKWS1
Known GenesTERT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3021n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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