A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16481324



Internal ID18998198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10651184..10651184hg38UCSC Ensembl
chr17:10554501..10554501hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3657912
Supporting Variants
Samples
Known GenesMYH3
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)essv16481324
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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