A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6164178



Internal ID9141581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91255545..91257397hg38UCSC Ensembl
chr9:94017827..94019679hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381853
hg191853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657277
Supporting Variants
SamplesNA19376
Known GenesAUH
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6164178
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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