A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3688479



Internal ID19406487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99568067..99568067hg38UCSC Ensembl
chr7:99165690..99165690hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16472708
Samples
Known GenesZNF655
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)esv3688479
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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