A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6939880



Internal ID10047337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:97998767..97999098hg38UCSC Ensembl
Outerchr9:100761049..100761380hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738816
Supporting Variants
SamplesSSM022
Known GenesANP32B
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)essv6939880
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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