A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11187536



Internal ID862304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152081335..152082140hg38UCSC Ensembl
Innerchr3:152081352..152082123hg38UCSC Ensembl
Outerchr3:152081318..152082157hg38UCSC Ensembl
chr3:151799124..151799929hg19UCSC Ensembl
Innerchr3:151799141..151799912hg19UCSC Ensembl
Outerchr3:151799107..151799946hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38806
hg19806
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598198
Supporting Variants
SamplesHG00451
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11187536
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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