A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2633277



Internal ID8350149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:108048276..108049725hg38UCSC Ensembl
Outerchr3:107767123..107768572hg19UCSC Ensembl
Outerchr3:109249813..109251262hg18UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg381450
hg191450
hg181450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5290121
SamplesNA18507
Known GenesCD47
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)esv2633277
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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