A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10918304



Internal ID4298287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9860523..9864755hg38UCSC Ensembl
Innerchr3:9860544..9864734hg38UCSC Ensembl
Outerchr3:9860502..9864776hg38UCSC Ensembl
chr3:9902207..9906439hg19UCSC Ensembl
Innerchr3:9902228..9906418hg19UCSC Ensembl
Outerchr3:9902186..9906460hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg384233
hg194233
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595253
Supporting Variants
SamplesHG03857
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10918304
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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