A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6954877



Internal ID10063761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:110569550..110569965hg38UCSC Ensembl
Outerchr1:111112172..111112587hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716062, esv2716051
Supporting Variants
SamplesSSM026
Known Genes
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)essv6954877
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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