A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586151



Internal ID6973671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57916740..57918638hg38UCSC Ensembl
Innerchr1:57916776..57918602hg38UCSC Ensembl
Outerchr1:57916704..57918674hg38UCSC Ensembl
chr1:58382412..58384310hg19UCSC Ensembl
Innerchr1:58382448..58384274hg19UCSC Ensembl
Outerchr1:58382376..58384346hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg381899
hg191899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9938786
SamplesHG03611
Known GenesDAB1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586151
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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