A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16483062



Internal ID19346622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29013073..29013073hg38UCSC Ensembl
chr19:29503980..29503980hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3659842
Supporting Variants
Samples
Known GenesLOC100505835
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)essv16483062
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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