A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6932726



Internal ID10041829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:28520424..28520840hg38UCSC Ensembl
Outerchr18:26100388..26100804hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716908
Supporting Variants
SamplesSSM020
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)essv6932726
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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