A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2512242



Internal ID8575800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:45179865..45181878hg38UCSC Ensembl
Outerchr17:43257232..43259245hg19UCSC Ensembl
Outerchr17:40613015..40615028hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382014
hg192014
hg182014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5202569
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)esv2512242
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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