A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6592685



Internal ID9727542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82257282..82264389hg38UCSC Ensembl
chr9:84872197..84879304hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg387108
hg197108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668434
Supporting Variants
SamplesNA19651
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6592685
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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