A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2489412



Internal ID8552970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:3643172..3644834hg38UCSC Ensembl
Outerchr1:3559736..3561398hg19UCSC Ensembl
Outerchr1:3549596..3551258hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg381663
hg191663
hg181663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5381740
SamplesNA18507
Known GenesWRAP73
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)esv2489412
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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