A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6903514



Internal ID10015246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:36485926..36486182hg38UCSC Ensembl
Outerchr5:36486028..36486284hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2730080
Supporting Variants
SamplesSSM013
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)essv6903514
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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