A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2500362



Internal ID8563920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:150180851..150182184hg38UCSC Ensembl
Outerchr3:149898638..149899971hg19UCSC Ensembl
Outerchr3:151381328..151382661hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg381334
hg191334
hg181334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5211093
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)esv2500362
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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