A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6691329



Internal ID9757771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:37336713..37371218hg38UCSC Ensembl
Outerchr10:37625641..37660146hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3834506
hg1934506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2735584, esv2735517
Supporting Variants
SamplesSSM036
Known GenesLINC00993
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)essv6691329
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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