A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2610614



Internal ID8674173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:18993620..18994625hg38UCSC Ensembl
Outerchr3:19035112..19036117hg19UCSC Ensembl
Outerchr3:19010116..19011121hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38285
hg19285
hg18285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5350147
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)esv2610614
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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