A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6927532



Internal ID9690176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:93010420..93010850hg38UCSC Ensembl
Outerchr9:95772702..95773132hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38431
hg19431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738777
Supporting Variants
SamplesSSM019
Known GenesFGD3
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)essv6927532
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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