A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2737337



Internal ID9971675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:96787613..96788232hg38UCSC Ensembl
Outerchr8:97799841..97800460hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6881906, essv6850228, essv6749243, essv6879082, essv6740557, essv6873269, essv6672163, essv6755075, essv6705683, essv6976027, essv6775178, essv6760556, essv6935442, essv6814922, essv6964804, essv6958200
SamplesSSM027, SSM086, SSM091, SSM061, SSM040, SSM031, SSM094, SSM077, SSM093, SSM056, SSM066, SSM029, SSM021, SSM052, SSM026, SSM058
Known GenesCPQ
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)esv2737337
Frequency
Sample Size96
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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