A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6174396



Internal ID9151799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69536167..69538113hg38UCSC Ensembl
chr9:72151083..72153029hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg381947
hg191947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663143
Supporting Variants
SamplesNA12777
Known GenesAPBA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6174396
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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