A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6958801



Internal ID10061263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97829848..97829928hg38UCSC Ensembl
Outerchr10:99589605..99589685hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739940, esv2739951
Supporting Variants
SamplesSSM026
Known GenesLINC00866
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)essv6958801
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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