A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6688022



Internal ID9755218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:24988670..24988812hg38UCSC Ensembl
Outerchr10:25277599..25277741hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734151, esv2734162
Supporting Variants
SamplesSSM035
Known GenesENKUR
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)essv6688022
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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