A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2910n106



Internal ID20162267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138044946..138046065hg38UCSC Ensembl
chr4:138966100..138967219hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg381120
hg191120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1127415, nsv1138145, nsv1119434
SamplesKWS1
Known GenesLINC00616
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2910n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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