A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6873444



Internal ID9922896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:29323990..29341740hg38UCSC Ensembl
Outerchr10:29612919..29630669hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3817751
hg1917751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734606, esv2734917
Supporting Variants
SamplesSSM091
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)essv6873444
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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