A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586786



Internal ID6974304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91034694..91042296hg38UCSC Ensembl
Innerchr1:91034711..91042280hg38UCSC Ensembl
Outerchr1:91034678..91042313hg38UCSC Ensembl
chr1:91500251..91507853hg19UCSC Ensembl
Innerchr1:91500268..91507837hg19UCSC Ensembl
Outerchr1:91500235..91507870hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg387603
hg197603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10012254
SamplesNA21091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586786
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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