A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16488652



Internal ID19005526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42969587..42969587hg38UCSC Ensembl
chr1:43435258..43435258hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3666054
Supporting Variants
Samples
Known GenesSLC2A1-AS1
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)essv16488652
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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