A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586153



Internal ID6973673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58102219..58116075hg38UCSC Ensembl
Innerchr1:58102719..58115575hg38UCSC Ensembl
Outerchr1:58101219..58117075hg38UCSC Ensembl
chr1:58567891..58581747hg19UCSC Ensembl
Innerchr1:58568391..58581247hg19UCSC Ensembl
Outerchr1:58566891..58582747hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3813857
hg1913857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9938788
SamplesHG02425
Known GenesDAB1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586153
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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