A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3682431



Internal ID19400439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45277839..45277986hg38UCSC Ensembl
chr15:45570037..45570184hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16503391
Samples
Known Genes
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)esv3682431
Frequency
Sample Size20
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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