A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595528



Internal ID6982846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21873938..21933056hg38UCSC Ensembl
Innerchr3:21873938..21933056hg38UCSC Ensembl
Outerchr3:21873438..21933556hg38UCSC Ensembl
chr3:21915430..21974548hg19UCSC Ensembl
Innerchr3:21915430..21974548hg19UCSC Ensembl
Outerchr3:21914930..21975048hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3859119
hg1959119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10948019
SamplesHG01366
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595528
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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