A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2748039



Internal ID10329009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:110677075..110677691hg38UCSC Ensembl
Outerchr13:111329422..111330038hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6846115, essv6894848, essv6685280, essv6772281, essv6728527, essv6842652, essv6720901, essv6796241, essv6673507, essv6920424, essv6882490, essv6702673, essv6732337, essv6724694, essv6706402, essv6945183, essv6857558, essv6815637, essv6779656
SamplesSSM071, SSM045, SSM046, SSM065, SSM087, SSM039, SSM023, SSM084, SSM047, SSM017, SSM094, SSM031, SSM067, SSM044, SSM085, SSM040, SSM077, SSM034, SSM098
Known GenesCARS2
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)esv2748039
Frequency
Sample Size96
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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