A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3664319



Internal ID19382327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21558875..21558875hg38UCSC Ensembl
chr3:21600367..21600367hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16487091
Samples
Known GenesZNF385D
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)esv3664319
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer