A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9892209



Internal ID659197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25045102..25047737hg38UCSC Ensembl
Innerchr1:25045132..25047707hg38UCSC Ensembl
Outerchr1:25045072..25047767hg38UCSC Ensembl
chr1:25371593..25374228hg19UCSC Ensembl
Innerchr1:25371623..25374198hg19UCSC Ensembl
Outerchr1:25371563..25374258hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382636
hg192636
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585518
Supporting Variants
SamplesHG00306
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9892209
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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