A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2743698



Internal ID10324668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132569909..132570165hg38UCSC Ensembl
Outerchr10:134383413..134383669hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6706017, essv6856868
SamplesSSM087, SSM040
Known GenesINPP5A
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)esv2743698
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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