A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595527



Internal ID6982845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21844397..21867786hg38UCSC Ensembl
Innerchr3:21844397..21867786hg38UCSC Ensembl
Outerchr3:21844237..21868015hg38UCSC Ensembl
chr3:21885889..21909278hg19UCSC Ensembl
Innerchr3:21885889..21909278hg19UCSC Ensembl
Outerchr3:21885729..21909507hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3823390
hg1923390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv877e214
Supporting Variantsessv10948017, essv10948018
SamplesHG01366, HG03744
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595527
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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