A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6944498



Internal ID9706419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1558425..1558785hg38UCSC Ensembl
Outerchr10:1600620..1600980hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2730173, esv2730162
Supporting Variants
SamplesSSM023
Known GenesADARB2
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)essv6944498
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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