A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6855713



Internal ID9906938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101034754..101036567hg38UCSC Ensembl
Outerchr7:100678035..100679848hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381814
hg191814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734914, esv2734888, esv2734913
Supporting Variants
SamplesSSM087
Known GenesMUC17
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)essv6855713
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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