A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10980893



Internal ID1389970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36354776..36375423hg38UCSC Ensembl
Innerchr3:36354779..36375421hg38UCSC Ensembl
Outerchr3:36354774..36375426hg38UCSC Ensembl
chr3:36396268..36416915hg19UCSC Ensembl
Innerchr3:36396271..36416913hg19UCSC Ensembl
Outerchr3:36396266..36416918hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3820648
hg1920648
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595856
Supporting Variants
SamplesHG01257
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10980893
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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