A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6832632



Internal ID10006410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35742919..35743171hg38UCSC Ensembl
Outerchr10:36031847..36032099hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2735439, esv2735428
Supporting Variants
SamplesSSM010
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)essv6832632
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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