A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2748399



Internal ID9982683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113830370..113830655hg38UCSC Ensembl
Outerchr13:114533343..114533628hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6867470, essv6673568, essv6812395, essv6851599, essv6685302, essv6732370, essv6772315, essv6788026, essv6783814, essv6879654, essv6891482, essv6888186, essv6901488, essv6971094, essv6720937
SamplesSSM065, SSM097, SSM093, SSM028, SSM047, SSM069, SSM096, SSM089, SSM031, SSM044, SSM086, SSM068, SSM076, SSM034, SSM012
Known GenesGAS6, GAS6-AS1
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)esv2748399
Frequency
Sample Size96
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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