A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596403



Internal ID6983718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64298066..64300569hg38UCSC Ensembl
Innerchr3:64298078..64300557hg38UCSC Ensembl
Outerchr3:64298054..64300581hg38UCSC Ensembl
chr3:64283742..64286245hg19UCSC Ensembl
Innerchr3:64283754..64286233hg19UCSC Ensembl
Outerchr3:64283730..64286257hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg382504
hg192504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11029201
SamplesHG03127
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596403
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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