A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6686561



Internal ID9756301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:2269926..2270303hg38UCSC Ensembl
Outerchr3:2311610..2311987hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2724793, esv2724792
Supporting Variants
SamplesSSM035
Known GenesCNTN4
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)essv6686561
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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