A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2461269



Internal ID8178141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:32663170..32664688hg38UCSC Ensembl
Outerchr10:32952098..32953616hg19UCSC Ensembl
Outerchr10:32992104..32993622hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381519
hg191519
hg181519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5344108
SamplesNA18507
Known GenesCCDC7
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)esv2461269
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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