A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6935711



Internal ID9697805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1298742..1298977hg38UCSC Ensembl
Outerchr10:1340937..1341172hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2729662
Supporting Variants
SamplesSSM021
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)essv6935711
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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