A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9893320



Internal ID5209228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25573793..25581616hg38UCSC Ensembl
Innerchr1:25573793..25581616hg38UCSC Ensembl
Outerchr1:25573531..25581894hg38UCSC Ensembl
chr1:25900284..25908107hg19UCSC Ensembl
Innerchr1:25900284..25908107hg19UCSC Ensembl
Outerchr1:25900022..25908385hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg387824
hg197824
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585530
Supporting Variants
SamplesNA18618
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9893320
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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