A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16475930



Internal ID19339490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89350311..89350311hg38UCSC Ensembl
chr10:91110068..91110068hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3651918
Supporting Variants
Samples
Known Genes
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)essv16475930
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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