A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16467899



Internal ID19331459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57631725..57632022hg38UCSC Ensembl
chr3:57617452..57617749hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3683135
Supporting Variants
Samples
Known GenesDENND6A
MethodSequencing
Analysisde novo assemblies produced from SoapDenovo2 were aligned to GRC37 using LAST and input into SoapAsmVar for population-wide structural variation detection. The method is described in the publication
PlatformIllumina HiSeq 2000
Comments
ReferenceBesenbacher_et_al_2015
Pubmed ID25597990
Accession Number(s)essv16467899
Frequency
Sample Size20
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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