A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5210627



Internal ID8302362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:194834489..194836222hg38UCSC Ensembl
Outerchr3:194555218..194556951hg19UCSC Ensembl
Outerchr3:196036507..196038240hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381734
hg191734
hg181734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2451272
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)essv5210627
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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