A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6690693



Internal ID9760173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:33672224..33672629hg38UCSC Ensembl
Outerchr7:33711836..33712241hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734236, esv2734221, esv2734226
Supporting Variants
SamplesSSM036
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)essv6690693
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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