A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6396554



Internal ID9373957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114325228..114332005hg38UCSC Ensembl
chr9:117087508..117094285hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg386778
hg196778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664309
Supporting Variants
SamplesNA18873
Known GenesORM1, ORM2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6396554
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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