A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2731356



Internal ID9965673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:515329..515898hg38UCSC Ensembl
Outerchr6:515329..515898hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6848950, essv6822352, essv6739875, essv6778071, essv6830072, essv6793965, essv6872635, essv6907419, essv6767418, essv6963539, essv6886924, essv6690319
SamplesSSM027, SSM086, SSM036, SSM091, SSM064, SSM067, SSM009, SSM096, SSM079, SSM052, SSM014, SSM081
Known GenesEXOC2
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)esv2731356
Frequency
Sample Size96
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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