A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1269e201



Internal ID20126156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133827235..133828439hg38UCSC Ensembl
chr9:136692357..136693561hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381205
hg191205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2739186, esv2739183, esv2739188
SamplesSSM100, SSM036, SSM083, SSM071, SSM027, SSM024, SSM045, SSM046, SSM011, SSM079, SSM065, SSM087, SSM097, SSM039, SSM042, SSM088, SSM002, SSM057, SSM023, SSM028, SSM092, SSM084, SSM090, SSM021, SSM047, SSM069, SSM062, SSM026, SSM089, SSM019, SSM035, SSM032, SSM044, SSM001, SSM086, SSM033, SSM066, SSM085, SSM068, SSM081, SSM082, SSM020, SSM015, SSM078, SSM016, SSM053, SSM080, SSM037, SSM077, SSM022, SSM010, SSM070, SSM095, SSM025, SSM034, SSM004, SSM043, SSM098, SSM049, SSM012
Known GenesVAV2
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)dgv1269e201
Frequency
Sample Size96
Observed Gain0
Observed Loss60
Observed Complex0
Frequencyn/a


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