A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6173497



Internal ID9150900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62450945..62451477hg38UCSC Ensembl
chr11:62218417..62218949hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671635
Supporting Variants
SamplesNA20512
Known GenesAHNAK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6173497
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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