A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6936306



Internal ID10045373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:44141965..44142464hg38UCSC Ensembl
Outerchr13:44716101..44716600hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2747331
Supporting Variants
SamplesSSM021
Known GenesSMIM2-AS1
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)essv6936306
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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