A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3667463



Internal ID19385471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39217041..39217095hg38UCSC Ensembl
chr21:40588967..40589021hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16465963
Samples
Known GenesBRWD1
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)esv3667463
Frequency
Sample Size20
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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