A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2747866



Internal ID9982150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:98677985..98678402hg38UCSC Ensembl
Outerchr13:99330239..99330656hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6673478, essv6912802, essv6713175, essv6685256, essv6796230
SamplesSSM071, SSM042, SSM031, SSM015, SSM034
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)esv2747866
Frequency
Sample Size96
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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