A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16494311



Internal ID19011185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100918482..100918688hg38UCSC Ensembl
chr8:101930710..101930916hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3672343
Supporting Variants
Samples
Known GenesYWHAZ
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)essv16494311
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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