A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3678897



Internal ID19050219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140683024..140683082hg38UCSC Ensembl
chr7:140382824..140382882hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16500211
Samples
Known GenesADCK2
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)esv3678897
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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