A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6944607



Internal ID10053218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:91055635..91055960hg38UCSC Ensembl
Outerchr10:92815392..92815717hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739485
Supporting Variants
SamplesSSM023
Known GenesLINC00502
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)essv6944607
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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