A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595520



Internal ID6982838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21761907..21770697hg38UCSC Ensembl
Innerchr3:21761907..21770697hg38UCSC Ensembl
Outerchr3:21761827..21770729hg38UCSC Ensembl
chr3:21803399..21812189hg19UCSC Ensembl
Innerchr3:21803399..21812189hg19UCSC Ensembl
Outerchr3:21803319..21812221hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg388791
hg198791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10947999, essv10948000
SamplesNA18538, HG00611
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595520
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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