A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6901258



Internal ID9946884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79473478..79473745hg38UCSC Ensembl
Outerchr18:77233478..77233745hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717650, esv2717497, esv2717652
Supporting Variants
SamplesSSM100
Known GenesNFATC1
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)essv6901258
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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