A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5614608



Internal ID8592011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62477544..62482154hg38UCSC Ensembl
chr11:62245016..62249626hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg384611
hg194611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673066
Supporting Variants
SamplesNA07048
Known GenesAHNAK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5614608
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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