A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589775



Internal ID6977105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9560110..9561205hg38UCSC Ensembl
Innerchr2:9560173..9561142hg38UCSC Ensembl
Outerchr2:9560047..9561268hg38UCSC Ensembl
chr2:9700239..9701334hg19UCSC Ensembl
Innerchr2:9700302..9701271hg19UCSC Ensembl
Outerchr2:9700176..9701397hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381096
hg191096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10404370
SamplesHG01852
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589775
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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