A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2556372



Internal ID8273244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:67730240..67731899hg38UCSC Ensembl
Outerchr17:65726356..65728015hg19UCSC Ensembl
Outerchr17:63156818..63158477hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381660
hg191660
hg181660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5362335
SamplesNA18507
Known GenesNOL11
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)esv2556372
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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