A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5262099



Internal ID8007148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127734935..127735310hg38UCSC Ensembl
chr6:128056080..128056455hg19UCSC Ensembl
chr6:128097773..128098148hg18UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38376
hg19376
hg18376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2484840
Supporting Variants
SamplesNA18507
Known GenesTHEMIS
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)essv5262099
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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