A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674144



Internal ID9940249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71504013..71537497hg38UCSC Ensembl
Outerchr11:71503976..71537547hg38UCSC Ensembl
Innerchr11:71215059..71248543hg19UCSC Ensembl
Outerchr11:71215022..71248593hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3833572
hg1933572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5603928
SamplesHG00638
Known GenesKRTAP5-7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674144
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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