A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664106



Internal ID9583525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63922424..63924041hg38UCSC Ensembl
chr1:64388095..64389712hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381618
hg191618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5446559
SamplesHG01125
Known GenesROR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664106
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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