A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2444888



Internal ID8508446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:93786962..93794133hg38UCSC Ensembl
Outerchr7:93416274..93423445hg19UCSC Ensembl
Outerchr7:93254210..93261381hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg387172
hg197172
hg187172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5185642
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)esv2444888
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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