A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11038685



Internal ID1079762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72686424..72687533hg38UCSC Ensembl
Innerchr3:72686474..72687483hg38UCSC Ensembl
Outerchr3:72686370..72687587hg38UCSC Ensembl
chr3:72735575..72736684hg19UCSC Ensembl
Innerchr3:72735625..72736634hg19UCSC Ensembl
Outerchr3:72735521..72736738hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381110
hg191110
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596539
Supporting Variants
SamplesHG00704
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11038685
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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