A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3673860



Internal ID19045182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16731717..16731861hg38UCSC Ensembl
chr19:16842528..16842672hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16495678
Samples
Known GenesNWD1
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)esv3673860
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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