A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6921886



Internal ID10034562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:197924896..197925183hg38UCSC Ensembl
Outerchr1:197894026..197894313hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2721106, esv2721095, esv2721128
Supporting Variants
SamplesSSM018
Known GenesLHX9
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)essv6921886
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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