A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6264776



Internal ID9242179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127270879..127272536hg38UCSC Ensembl
chr9:130033158..130034815hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381658
hg191658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676607
Supporting Variants
SamplesNA19327
Known GenesGARNL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6264776
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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