A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2739233



Internal ID10322869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:134685151..134685700hg38UCSC Ensembl
Outerchr9:137576997..137577546hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6850546, essv6691260, essv6687976, essv6724111
SamplesSSM036, SSM045, SSM035, SSM086
Known GenesCOL5A1
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)esv2739233
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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