A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3657164



Internal ID19375172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24926125..24926125hg38UCSC Ensembl
chr16:24937446..24937446hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16480651
Samples
Known GenesARHGAP17
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)esv3657164
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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