A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11171236



Internal ID1199462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145719637..145779235hg38UCSC Ensembl
Innerchr3:145719637..145779235hg38UCSC Ensembl
Outerchr3:145719137..145779735hg38UCSC Ensembl
chr3:145437424..145497022hg19UCSC Ensembl
Innerchr3:145437424..145497022hg19UCSC Ensembl
Outerchr3:145436924..145497522hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3859599
hg1959599
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598075
Supporting Variants
SamplesHG01070
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11171236
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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