A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585541



Internal ID6973063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26504833..26513567hg38UCSC Ensembl
Innerchr1:26504883..26513517hg38UCSC Ensembl
Outerchr1:26504781..26513619hg38UCSC Ensembl
chr1:26831324..26840058hg19UCSC Ensembl
Innerchr1:26831374..26840008hg19UCSC Ensembl
Outerchr1:26831272..26840110hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg388735
hg198735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9893923, essv9893924
SamplesNA20768, NA20801
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585541
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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