A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6761849



Internal ID9823670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:13111958..13119868hg38UCSC Ensembl
Outerchr1:13179430..13187341hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg387911
hg197912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743964
Supporting Variants
SamplesSSM062
Known GenesHNRNPCP5
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)essv6761849
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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