A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6392189



Internal ID9369592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125445832..125447654hg38UCSC Ensembl
chr9:128208111..128209933hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381823
hg191823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659060
Supporting Variants
SamplesNA19712
Known GenesMAPKAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6392189
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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