A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6929865



Internal ID10039064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:6879630..6879871hg38UCSC Ensembl
Outerchr4:6881357..6881598hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2727009
Supporting Variants
SamplesSSM020
Known GenesKIAA0232
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)essv6929865
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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