A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2503667



Internal ID8567225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:28861796..28863530hg38UCSC Ensembl
Outerchr21:30234118..30235852hg19UCSC Ensembl
Outerchr21:29155989..29157723hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg381735
hg191735
hg181735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5177413
SamplesNA18507
Known Genes
MethodSequencing
AnalysisLarger insertions and deletions are found by looking at variation in mate pair distances in the 2x50 mate pair libraries. These data are included in separate files for each of three coverage values: 2.2x, 4.0x, 5.6x, and 8.4x
PlatformNot specified
CommentsoriginalFile=Yoruban_large_indels_8.4x.gff
ReferenceMcKernan_et_al_2009
Pubmed ID19546169
Accession Number(s)esv2503667
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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