A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6931493



Internal ID9694493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35150685..35151098hg38UCSC Ensembl
Outerchr10:35439613..35440026hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2735328
Supporting Variants
SamplesSSM020
Known GenesCREM
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)essv6931493
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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