A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9892050



Internal ID4206098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24776225..24777798hg38UCSC Ensembl
Innerchr1:24776228..24777796hg38UCSC Ensembl
Outerchr1:24776223..24777801hg38UCSC Ensembl
chr1:25102716..25104289hg19UCSC Ensembl
Innerchr1:25102719..25104287hg19UCSC Ensembl
Outerchr1:25102714..25104292hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381574
hg191574
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585514
Supporting Variants
SamplesHG03787
Known GenesCLIC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9892050
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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