A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3659777



Internal ID19377785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21168396..21168396hg38UCSC Ensembl
chr19:21351199..21351199hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16483003
Samples
Known GenesZNF431
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)esv3659777
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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