A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3688494



Internal ID19059816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100172890..100172890hg38UCSC Ensembl
chr7:99770513..99770513hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16472721
Samples
Known GenesGPC2
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)esv3688494
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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