A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6685196



Internal ID10098036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:26982826..26983168hg38UCSC Ensembl
Outerchr13:27556963..27557305hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2747178
Supporting Variants
SamplesSSM034
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)essv6685196
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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