A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6298044



Internal ID9275447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105729439..105732667hg38UCSC Ensembl
chr9:108491720..108494948hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg383229
hg193229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675392
Supporting Variants
SamplesNA18606
Known GenesTMEM38B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6298044
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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