A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6499166



Internal ID9476569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201841512..201846520hg38UCSC Ensembl
chr1:201810640..201815648hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg385009
hg195009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667793
Supporting Variants
SamplesHG00403
Known GenesIPO9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6499166
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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