A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586165



Internal ID6973685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58424291..58432923hg38UCSC Ensembl
Innerchr1:58424292..58432922hg38UCSC Ensembl
Outerchr1:58424290..58432924hg38UCSC Ensembl
chr1:58889963..58898595hg19UCSC Ensembl
Innerchr1:58889964..58898594hg19UCSC Ensembl
Outerchr1:58889962..58898596hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg388633
hg198633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9941820
SamplesNA18612
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586165
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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