A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3681167



Internal ID19399175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101652289..101652375hg38UCSC Ensembl
chr8:102664517..102664603hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16502255
Samples
Known GenesGRHL2
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)esv3681167
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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