A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6159195



Internal ID9136598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62528558..62528759hg38UCSC Ensembl
chr11:62296030..62296231hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661679
Supporting Variants
SamplesHG01072
Known GenesAHNAK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6159195
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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