A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3296n106



Internal ID20162653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28510223..28623423hg38UCSC Ensembl
chr6:28478000..28591200hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38113201
hg19113201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1112898, nsv1126747
SamplesKWS1, KWS2
Known GenesGPX5, GPX6, SCAND3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3296n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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