A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6861986



Internal ID9911715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:37336707..37371129hg38UCSC Ensembl
Outerchr10:37625635..37660057hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3834423
hg1934423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2735584, esv2735517
Supporting Variants
SamplesSSM088
Known GenesLINC00993
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)essv6861986
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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