A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6958935



Internal ID10061383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133113052..133113126hg38UCSC Ensembl
Outerchr10:134926556..134926630hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743825, esv2743824
Supporting Variants
SamplesSSM026
Known GenesGPR123
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)essv6958935
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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