A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589827



Internal ID6977157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11981510..11992461hg38UCSC Ensembl
Innerchr2:11981660..11992311hg38UCSC Ensembl
Outerchr2:11981360..11992611hg38UCSC Ensembl
chr2:12121636..12132587hg19UCSC Ensembl
Innerchr2:12121786..12132437hg19UCSC Ensembl
Outerchr2:12121486..12132737hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3810952
hg1910952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10410489
SamplesNA19338
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589827
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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