A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3666829



Internal ID19384837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52323895..52323895hg38UCSC Ensembl
chr1:52789567..52789567hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16489350
Samples
Known GenesZFYVE9
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)esv3666829
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