A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3358n106



Internal ID20162715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106535747..106536066hg38UCSC Ensembl
chr6:106983622..106983941hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1116812, nsv1130105, nsv1121350
SamplesKWS1, KWS2
Known GenesAIM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3358n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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