A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596839



Internal ID6984153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85382391..85446222hg38UCSC Ensembl
Innerchr3:85382891..85445722hg38UCSC Ensembl
Outerchr3:85381391..85447222hg38UCSC Ensembl
chr3:85431541..85495372hg19UCSC Ensembl
Innerchr3:85432041..85494872hg19UCSC Ensembl
Outerchr3:85430541..85496372hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3863832
hg1963832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11061871, essv11061870
SamplesHG02154, HG03685
Known GenesCADM2, MIR5688
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596839
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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