A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6923848



Internal ID9686482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:93010449..93010877hg38UCSC Ensembl
Outerchr9:95772731..95773159hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738777
Supporting Variants
SamplesSSM018
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)essv6923848
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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