A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6686222



Internal ID9756606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:111544837..111545043hg38UCSC Ensembl
Outerchr1:112087459..112087665hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716274, esv2716252
Supporting Variants
SamplesSSM035
Known GenesADORA3
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)essv6686222
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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