A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6799796



Internal ID9855228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133977784..133978166hg38UCSC Ensembl
Outerchr9:136842906..136843288hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739194, esv2739138
Supporting Variants
SamplesSSM072
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)essv6799796
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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