A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6976564



Internal ID10081562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:44414476..44414594hg38UCSC Ensembl
Outerchr10:44909924..44910042hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2735939, esv2735928
Supporting Variants
SamplesSSM029
Known Genes
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)essv6976564
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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