A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5176771



Internal ID7921820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:85433995..85435385hg38UCSC Ensembl
Outerchr6:86143713..86145103hg19UCSC Ensembl
Outerchr6:86200432..86201822hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg381391
hg191391
hg181391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2448290
Supporting Variants
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)essv5176771
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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