A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2550334



Internal ID8613892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171618752..171618858hg38UCSC Ensembl
chr3:171336542..171336648hg19UCSC Ensembl
chr3:172819236..172819342hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38107
hg19107
hg18107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5275754
SamplesNA18507
Known GenesPLD1
MethodSequencing
AnalysisThe small_indels files contain insertions and deletions detected using the AB Small indel tool. After individual sequence tags from fragment and 2x25 mate pair data are matched to the reference, insertion of up to 3 bases and deletions of up to 11 bases are reported. Somewhat larger indels (12-500 bp) can be detected in the 2x50 mate pair data and these are included as well (Yoruban_med_ins_04_14.gff, Yoruban_med_ins_15_19.gff, Yoruban_med_del_12_500.gff). Small and medium indel files include a number of name=value attributes as described in the small indel tool manual.
PlatformNot specified
CommentsoriginalFile=Yoruban_med_del_12_500.gff
ReferenceMcKernan_et_al_2009
Pubmed ID19546169
Accession Number(s)esv2550334
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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