A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5237168



Internal ID8328903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:76324507..76326013hg38UCSC Ensembl
Outerchr3:76373658..76375164hg19UCSC Ensembl
Outerchr3:76456348..76457854hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381507
hg191507
hg181507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2519372
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)essv5237168
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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