A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6763122



Internal ID9822744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:121077448..121078043hg38UCSC Ensembl
Outerchr9:123839726..123840321hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738997
Supporting Variants
SamplesSSM062
Known Genes
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)essv6763122
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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