A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586901



Internal ID6974329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98411746..98563044hg38UCSC Ensembl
chr1:98877302..99028600hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38151299
hg19151299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10026807
SamplesNA19083
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586901
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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