A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10954062



Internal ID1965039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25357505..25369088hg38UCSC Ensembl
Innerchr3:25357525..25369068hg38UCSC Ensembl
Outerchr3:25357485..25369108hg38UCSC Ensembl
chr3:25398996..25410579hg19UCSC Ensembl
Innerchr3:25399016..25410559hg19UCSC Ensembl
Outerchr3:25398976..25410599hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3811584
hg1911584
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595604
Supporting Variants
SamplesHG01815
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10954062
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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