A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595523



Internal ID6982841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21795344..21830985hg38UCSC Ensembl
Innerchr3:21795344..21830985hg38UCSC Ensembl
Outerchr3:21794844..21831485hg38UCSC Ensembl
chr3:21836836..21872477hg19UCSC Ensembl
Innerchr3:21836836..21872477hg19UCSC Ensembl
Outerchr3:21836336..21872977hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3835642
hg1935642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv876e214
Supporting Variantsessv10948005, essv10948006
SamplesHG01366, NA20809
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595523
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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