A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586183



Internal ID6626496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59423863..59469485hg38UCSC Ensembl
Innerchr1:59423863..59469485hg38UCSC Ensembl
Outerchr1:59423363..59469985hg38UCSC Ensembl
chr1:59889535..59935157hg19UCSC Ensembl
Innerchr1:59889535..59935157hg19UCSC Ensembl
Outerchr1:59889035..59935657hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3845623
hg1945623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9943924
SamplesHG03681
Known GenesFGGY
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586183
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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