A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11191928



Internal ID6852196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155945725..155953299hg38UCSC Ensembl
Innerchr3:155945759..155953265hg38UCSC Ensembl
Outerchr3:155945691..155953333hg38UCSC Ensembl
chr3:155663514..155671088hg19UCSC Ensembl
Innerchr3:155663548..155671054hg19UCSC Ensembl
Outerchr3:155663480..155671122hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg387575
hg197575
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598291
Supporting Variants
SamplesNA21088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11191928
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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