A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16480113



Internal ID18996987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70861402..70861402hg38UCSC Ensembl
chr15:71153741..71153741hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3656566
Supporting Variants
Samples
Known GenesLRRC49
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)essv16480113
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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