A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6894364



Internal ID10288410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:11885300..11885663hg38UCSC Ensembl
Outerchr10:11927299..11927662hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2733017
Supporting Variants
SamplesSSM098
Known GenesPROSER2-AS1
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)essv6894364
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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