A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3406n106



Internal ID22797234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141432357..141432457hg38UCSC Ensembl
chr6:141753494..141753594hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1124126, nsv1128277
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3406n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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