A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585577



Internal ID6973099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28298923..28300570hg38UCSC Ensembl
Innerchr1:28298973..28300520hg38UCSC Ensembl
Outerchr1:28298794..28300699hg38UCSC Ensembl
chr1:28625434..28627081hg19UCSC Ensembl
Innerchr1:28625484..28627031hg19UCSC Ensembl
Outerchr1:28625305..28627210hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381648
hg191648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9894724
SamplesHG01841
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585577
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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