A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1043e201



Internal ID11594887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168391508..168392209hg38UCSC Ensembl
chr6:168792188..168792889hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2733355, esv2733357
SamplesSSM065, SSM027, SSM082, SSM036, SSM043, SSM025, SSM071, SSM016, SSM039, SSM024, SSM045, SSM083, SSM077, SSM066, SSM028, SSM047, SSM069, SSM037, SSM046, SSM019, SSM096, SSM023, SSM079, SSM068, SSM015, SSM026, SSM070, SSM080
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)dgv1043e201
Frequency
Sample Size96
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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