A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10932575



Internal ID3759493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14343528..14350725hg38UCSC Ensembl
Innerchr3:14343539..14350715hg38UCSC Ensembl
Outerchr3:14343518..14350736hg38UCSC Ensembl
chr3:14385028..14392225hg19UCSC Ensembl
Innerchr3:14385039..14392215hg19UCSC Ensembl
Outerchr3:14385018..14392236hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg387198
hg197198
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595367
Supporting Variants
SamplesHG03388
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10932575
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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