A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5319388



Internal ID8411123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:106125328..106126911hg38UCSC Ensembl
Outerchr9:108887609..108889192hg19UCSC Ensembl
Outerchr9:107927430..107929013hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381584
hg191584
hg181584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2600666
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)essv5319388
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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