A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9892041



Internal ID5273267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24728661..24734762hg38UCSC Ensembl
Innerchr1:24728661..24734762hg38UCSC Ensembl
Outerchr1:24728161..24735262hg38UCSC Ensembl
chr1:25055152..25061253hg19UCSC Ensembl
Innerchr1:25055152..25061253hg19UCSC Ensembl
Outerchr1:25054652..25061753hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386102
hg196102
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585511
Supporting Variants
SamplesNA18643
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9892041
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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