A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5211971



Internal ID7957020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:124942932..124944499hg38UCSC Ensembl
Outerchr9:127705211..127706778hg19UCSC Ensembl
Outerchr9:126745032..126746599hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381568
hg191568
hg181568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2442459
Supporting Variants
SamplesNA18507
Known GenesSCAI
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)essv5211971
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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