A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585530



Internal ID6973052
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9893321, essv9893318, essv9893322, essv9893319, essv9893320
SamplesNA18597, NA18618, NA18748, HG02128, NA19080
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585530
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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