A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11140889



Internal ID3643248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128944241..128946312hg38UCSC Ensembl
Innerchr3:128944259..128946295hg38UCSC Ensembl
Outerchr3:128944224..128946330hg38UCSC Ensembl
chr3:128663084..128665155hg19UCSC Ensembl
Innerchr3:128663102..128665138hg19UCSC Ensembl
Outerchr3:128663067..128665173hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382072
hg192072
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597728
Supporting Variants
SamplesHG03238
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11140889
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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